Identity
- Trade Name
- AccuThrive® FDA UDI
- Generic Name
- Microtome blade IVD, single-use FDA UDI
- Device Name
- AccuThrive Agility Microtome Blade Low Profile SS Microcoat 500BL/CA (50BL/DISP 10 DISP/CA) FDA UDI
- Model / Reference
- Microtome Blade FDA UDI
- Description
- AccuThrive Agility Microtome Blade Low Profile SS Microcoat 500BL/CA (50BL/DISP 10 DISP/CA) FDA UDI
Identifiers
- Catalog Number
- AVBL-2007-0000 FDA UDI
- Primary DI / UDI-DI
- 00843382104009 FDA UDI
- FDA Product Code
- IDL FDA UDI
- GMDN Term
- Microtome blade IVD, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3010 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Microtome blade IVD, single-use
AccuThrive® by AccuTec, Inc. — 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
- AccuTec, Inc.
Sources (1)
- FDA UDI e79755af-0cb2-4261-81b3-6020e25d762d 35 fields · synced Jun 1, 2026