Identity
- Trade Name
- Tissue-Tek® Accu-Edge® FDA UDI
- Generic Name
- Dissection board FDA UDI
- Device Name
- Dissecting Board FDA UDI
- Model / Reference
- 0159 FDA UDI
- Description
- Dissecting Board FDA UDI
Identifiers
- Catalog Number
- 0159 FDA UDI
- Primary DI / UDI-DI
- 00615233012661 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Dissection board 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
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
Yes
FDA UDI
Category: Dissection board
Tissue-Tek® Accu-Edge® by Sakura Finetek USA, 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
- Sakura Finetek USA, Inc
Sources (1)
- FDA UDI 37cc99ce-2294-4ba3-b79e-c117a627ae8c 35 fields · synced May 29, 2026