Identity
- Trade Name
- 3M™ ESPE™ FDA UDI
- Generic Name
- Oropharyngeal mucosa protection material FDA UDI
- Device Name
- 3M™ ESPE™ Xerostomia Relief Spray, 2 Canisters/Pack, 12137 FDA UDI
- Model / Reference
- 12137 FDA UDI
- Description
- 3M™ ESPE™ Xerostomia Relief Spray, 2 Canisters/Pack, 12137 FDA UDI
Identifiers
- Catalog Number
- 12137 FDA UDI
- Primary DI / UDI-DI
- 30348878600023 FDA UDI
- FDA Product Code
- LFD FDA UDI
- GMDN Term
- Oropharyngeal mucosa protection material FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
3m™ Espe™ by 3m Company — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI d8bb98b2-e479-426b-905c-94bc8def652e 36 fields · synced May 30, 2026