Identity
- Trade Name
- Facet Medical Technologies FDA UDI
- Generic Name
- Manual blood lancing device, reusable FDA UDI
- Device Name
- FMT Lancer Kit, CE FDA UDI
- Model / Reference
- 0108001 FDA UDI
- Description
- FMT Lancer Kit, CE FDA UDI
Identifiers
- Catalog Number
- 0108001 FDA UDI
- Primary DI / UDI-DI
- 00894743001338 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Manual blood lancing device, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual blood lancing device, reusable
Facet Medical Technologies by Facet Technologies, LLC. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Accu-Chek Fastclix — ROCHE DIABETES CARE, INC. · Class II
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
- Facet Technologies, LLC.
Sources (1)
- FDA UDI aa18e1e0-307a-4ce5-bf92-47c888d43ebd 35 fields · synced May 30, 2026