Identity
- Trade Name
- 3M™ Snap™ FDA UDI
- Generic Name
- Negative-pressure wound therapy system dressing set FDA UDI
- Device Name
- 3M™ Snap™ Therapy Strap, STPAM, Medium, 1 Each/Case FDA UDI
- Model / Reference
- STPAM FDA UDI
- Description
- 3M™ Snap™ Therapy Strap, STPAM, Medium, 1 Each/Case FDA UDI
Identifiers
- Catalog Number
- STPAM FDA UDI
- Primary DI / UDI-DI
- 00849554005556 FDA UDI
- FDA Product Code
- OKO FDA UDI
- GMDN Term
- Negative-pressure wound therapy system dressing set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4683 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
3M™ Snap™ by Kci Usa, 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
- Kci Usa, Inc.
Sources (1)
- FDA UDI e75031e8-0279-4888-94aa-984bb6c71b70 36 fields · synced May 29, 2026