Identity
- Trade Name
- 3M™ Reston™ FDA UDI
- Generic Name
- Multifunction body cushion FDA UDI
- Device Name
- 3M™ Reston™ Self-Adhering Foam Pads, 2851H, High Support, 6 1/4 in x 7 7/8 in (15/16 in Thick), 20/Case FDA UDI
- Model / Reference
- 2851H FDA UDI
- Description
- 3M™ Reston™ Self-Adhering Foam Pads, 2851H, High Support, 6 1/4 in x 7 7/8 in (15/16 in Thick), 20/Case FDA UDI
Identifiers
- Catalog Number
- 2851H FDA UDI
- Primary DI / UDI-DI
- 30707387789085 FDA UDI
- FDA Product Code
- FMP FDA UDI
- GMDN Term
- Multifunction body cushion FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6450 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multifunction body cushion
3M™ Reston™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI df06ed46-e4de-4da9-8500-704d45606afa 35 fields · synced Jun 6, 2026