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Align® RS Retropubic/Suprapubic Urethral Support System without Dilator
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Align® RS Retropubic/Suprapubic Urethral Support System without Dilator FDA UDI
- Generic Name
- Female stress urinary incontinence surgical mesh-sling, synthetic polymer FDA UDI
- Device Name
- ALIGN®Urethral Support System, Retropubic & Suprapubic w/o dilator FDA UDI
- Model / Reference
- BRD301RS FDA UDI
- Description
- ALIGN®Urethral Support System, Retropubic & Suprapubic w/o dilator FDA UDI
Identifiers
- Catalog Number
- BRD301RS FDA UDI
- Primary DI / UDI-DI
- 00801741016202 FDA UDI
- FDA Product Code
- OTN FDA UDI
- GMDN Term
- Female stress urinary incontinence surgical mesh-sling, synthetic polymer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 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
Yes
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
No
FDA UDI
Align® RS Retropubic/Suprapubic Urethral Support System without Dilator by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID
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
- C. R. Bard, Inc.
Sources (1)
- FDA UDI 60cab4fc-3daf-47e0-ae34-3b4bc6fec3a1 36 fields · synced May 31, 2026