Identity
- Trade Name
- Spectra FDA UDI
- Generic Name
- Rigid penile prosthesis FDA UDI
- Device Name
- Concealable Penile Prosthesis, 2 Cylinders FDA UDI
- Model / Reference
- 720074-02 FDA UDI
- Description
- Concealable Penile Prosthesis, 2 Cylinders FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00878953005287 FDA UDI
- FDA Product Code
- FAE FDA UDI
- GMDN Term
- Rigid penile prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.3630 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 12 Millimeter FDA UDILength — 16 Centimeter FDA UDI
Spectra by American Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- American Medical Systems, Inc.
Sources (1)
- FDA UDI c87b334f-2c5b-4dc7-a612-12a8e96b745b 35 fields · synced May 30, 2026