Identity
- Trade Name
- 3M™ Filtek™ FDA UDI
- Generic Name
- Dental matrix band, single-use FDA UDI
- Device Name
- 3M™ Filtek™ Matrix Lower Anterior, 1-2 Units, 749-212, 1 matrix/ plastic bag FDA UDI
- Model / Reference
- 749-212 FDA UDI
- Description
- 3M™ Filtek™ Matrix Lower Anterior, 1-2 Units, 749-212, 1 matrix/ plastic bag FDA UDI
Identifiers
- Catalog Number
- 749-212 FDA UDI
- Primary DI / UDI-DI
- 00652221300102 FDA UDI
- FDA Product Code
- EHY FDA UDI
- GMDN Term
- Dental matrix band, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6880 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
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
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: Dental matrix band, single-use
3M™ Filtek™ 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 e300b757-6786-43bd-9616-535b1dc527a3 35 fields · synced Jun 8, 2026