Identity
- Trade Name
- ACell® FDA UDI
- Generic Name
- Pelvic organ prolapse/stress urinary incontinence surgical mesh FDA UDI
- Device Name
- Pelvic Floor Matrix 5 x 5 cm FDA UDI
- Model / Reference
- PFM0505 FDA UDI
- Description
- Pelvic Floor Matrix 5 x 5 cm FDA UDI
Identifiers
- Catalog Number
- PFM0505 FDA UDI
- Primary DI / UDI-DI
- 00386190001264 FDA UDI
- FDA Product Code
- OXH FDA UDIFTM FDA UDI
- GMDN Term
- Pelvic organ prolapse/stress urinary incontinence surgical mesh 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Width — 5 Centimeter FDA UDILength — 5 Centimeter FDA UDI
ACell® by Acell, 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
- Acell, Inc.
Sources (1)
- FDA UDI 9334ccf8-d861-449e-be8b-9aff2151807c 38 fields · synced Jun 1, 2026