ZSI 475 FTM Inflatable Penile Implant
A single-cylinder hydraulic penile implant with pubic bone fixation for the neophallus after phalloplasty.
Product detail →Surgical Implant Inflatable penile implant
A three-piece hydraulic penile implant developed for the surgical treatment of erectile dysfunction. Two cylinders placed in the corpora cavernosa, a manual pump in the scrotum and a pelvic reservoir provide controlled inflation and deflation that mimics a natural erection. This content is institutional technical information for healthcare professionals and procurement teams; it is not patient guidance or treatment advice.
01 Overview
ZSI 475 is an inflatable penile implant manufactured by Zephyr Surgical Implants, based in Switzerland. It is used in the surgical treatment of erectile dysfunction caused by limited blood flow to the penis or by damaged nerves. Thanks to its three-component hydraulic architecture, the erection is initiated and ended under the patient's control in a way that closely follows the natural physiological cycle.
The two inflatable cylinders are implanted within the corpora cavernosa residing on either side of the penis; no tissue is removed to position them. The saline-filled reservoir is implanted in the pelvis and the manual pump in the scrotum. The patient presses the pump to transfer fluid from the reservoir into the cylinders; pressing the valve at the top of the pump returns the fluid to the reservoir and the penis becomes flaccid again.
The system remains entirely inside the body and is not visible externally. According to the manufacturer's documentation, the device does not affect the patient's capacity to urinate or ejaculate, nor the natural sensitivity of the penis and glans. Lisa Health provides documented supply of the ZSI penile implant portfolio, sizing planning support and operating-room preparation documentation to hospitals and urology teams. Clinical decisions and determination of indication rest solely with the specialist physician.
02 Clinical indications
The ZSI 475 is positioned for cases of erectile dysfunction that require a mechanical and durable solution. The headings below summarise frequently assessed clinical contexts; final indication, timing and patient suitability are determined solely by the urology/andrology team.
Contraindications and the assessment of active urinary or systemic infection, uncontrolled diabetes, insufficient tissue perfusion, patient manual dexterity and compliance are addressed within the current instructions for use and clinical protocols.
03 Structure and components
The ZSI 475 operates as a closed hydraulic circuit. Fluid is transferred between the reservoir and the cylinders via the pump; the entire system is implanted and requires no external component.
04 Kit and sizing coverage
The ZSI 475 is supplied as a complete kit containing all single-use instruments. Because all standard penile implant lengths and accessories are in the same box, a change of size in the operating room does not require an additional order or waiting time; this structure is designed to reduce stock and logistics burden.
| Parameter | Value | Clinical note |
|---|---|---|
| Number of cylinders | 2 | One cylinder per corpus cavernosum |
| Standard kit coverage | Corpora cavernosa 12 – 24 cm | All standard lengths in one box |
| Coverage with extenders | 24 cm and above | Rear tip extenders included in the kit |
| Special kit (ZSI 475-22) | Corpora cavernosa 21 – 25 cm | Supplied in a separate box for large anatomies |
| Rigidity resistance | > 500 g | Per manufacturer data, above the minimum pressure required for penetration |
| Reservoir | Pelvic, saline-filled | Sufficient volume for the inflation/deflation cycle |
| Pump | Scrotal manual pump | Deflation via the valve at the top |
| Coating | Hydrophilic PVP | Intended to improve antibiotic absorption |
| Instrumentation | Single-use, included in the kit | No additional tool required for assembly |
Dimensions and kit contents are compiled from the manufacturer's catalogue; final values are confirmed through the official product documentation and current instructions for use shared with the institution.
05 Operating principle
Operation is single-handed and requires no external component. Fluid is transferred between the reservoir and the cylinders within the closed circuit.
06 Distinguishing advantages
07 Comparison
The two products share the same hydraulic principle but are designed for different anatomies and different indications; they are not interchangeable. The table below compares the two versions for institutional assessment; the clinical preference rests with the specialist physician.
| Criterion | ZSI 475 | ZSI 475 FTM |
|---|---|---|
| Indication | Erectile dysfunction (natural penile anatomy) | Neophallus after phalloplasty |
| Number of cylinders | 2 — one per corpus cavernosum | 1 — a single cylinder in the neophallus |
| Placement | Within the corpora cavernosa | Within the neophallus |
| Proximal fixation | Stabilisation through corporal anatomy | Steel + silicone plate on the pubic bone |
| Sizing approach | Corpora cavernosa 12–24 cm; longer with extenders | Cylinder lengths of 120 / 150 / 180 / 210 mm |
| Supply format | All lengths and instruments in one box | Pre-connected and pre-filled set |
| Rigidity | > 500 g pressure resistance | > 500 g pressure resistance |
| Warranty | 5 years | 1 year |
If a non-surgical option for erectile dysfunction is being considered, the Active3 penile vacuum device in the portfolio can be reviewed as a non-invasive alternative.
Review the details of the ZSI 475 FTM phalloplasty version →08 Technical summary
| Manufacturer / brand | Zephyr Surgical Implants (ZSI) — Geneva, Switzerland |
|---|---|
| Model | ZSI 475 (ZSI 475-22 special kit for large anatomies) |
| Product family | Surgical implant / penile implant |
| Product type | Three-piece inflatable (hydraulic) penile implant |
| Field of use | Surgical treatment of erectile dysfunction |
| Components | Two inflatable cylinders, scrotal manual pump, pelvic saline reservoir |
| Material | Medical-grade silicone elastomer; three-layer cylinder wall |
| Coating | Hydrophilic PVP (for antibiotic absorption) |
| Sizing coverage | Corpora cavernosa 12–24 cm; longer with extenders · special kit 21–25 cm |
| Rigidity | > 500 g pressure resistance |
| Kit contents | All standard lengths, accessories and single-use instruments in one box |
| Functional impact | Urination, ejaculation and penile/glans sensitivity unaffected; no tissue removed |
| Imaging compatibility | Safe use in medical scanners; not detected by airport scanners |
| Warranty | 5 years (manufacturer) |
| Regulatory status | CE-marked medical device; classification, ÜTS and TİTCK registration details are confirmed with the supply file |
| Documentation | CE certificates, instructions for use, sizing and kit file, surgical technique and training materials |
| Target audience | Urology/andrology physicians, procurement and tender departments |
09 Questions & answers
The ZSI 475 is considered in cases of erectile dysfunction caused by limited blood flow to the penis or by damaged nerves, where conservative treatments have not produced an adequate response. Indication, timing and patient suitability are determined solely by the urology/andrology team.
The standard kit covers corpora cavernosa from 12 cm to 24 cm, and longer anatomies are addressed with extenders. For cases with corpora cavernosa of 21–25 cm, the ZSI 475-22 special kit is supplied in a separate box. Final sizing is based on intraoperative corporal measurement.
The ZSI 475 is a two-cylinder system used for erectile dysfunction in natural penile anatomy with corpora cavernosa. The ZSI 475 FTM is a single-cylinder version developed for a neophallus created by phalloplasty and includes a pubic bone fixation plate. The two products have different indications and are not interchangeable.
According to the manufacturer's documentation, no tissue is removed when the cylinders are inserted into the corpora cavernosa, and the device does not affect the patient's capacity to urinate or ejaculate, nor the natural sensitivity of the penis and glans. Clinical assessment and patient information remain the physician's responsibility.
According to the manufacturer's documentation, the device cannot be detected by airport security scanners and is designed for safe use with medical imaging equipment. Confirming institutional protocol and the current instructions for use before imaging is recommended.
Kit contents, sizing and extender options, CE and ÜTS documents, lot/serial traceability and the surgical training plan are compiled according to the institution's procurement format. No public pricing is published; quotations are prepared per institution.
10 Related products
Review the complementary products in the ZSI surgical implant family and the erectile dysfunction portfolio.
Tell us your institution type, case profile and the documents you need; we will respond with kit contents, sizing coverage, surgical training and a quotation timeline.