Identity
- Trade Name
- Tissue-Tek® Accu-Edge® FDA UDI
- Generic Name
- Laboratory scale, electronic FDA UDI
- Device Name
- Scale, Digital FDA UDI
- Model / Reference
- 0204 FDA UDI
- Description
- Scale, Digital FDA UDI
Identifiers
- Catalog Number
- 0204 FDA UDI
- Primary DI / UDI-DI
- 00615233012753 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Laboratory scale, electronic 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laboratory scale, electronic
Tissue-Tek® Accu-Edge® by Sakura Finetek USA, Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Sakura Finetek USA, Inc
Sources (1)
- FDA UDI 00a5caa8-8c24-4eac-be2a-681f39e88d96 35 fields · synced Jun 8, 2026