Identity
- Trade Name
- Tissue-Tek VIP® FDA UDI
- Generic Name
- 37% Formaldehyde solution IVD FDA UDI
- Device Name
- Fixative, 2.5 Gallon Cube FDA UDI
- Model / Reference
- 5989 FDA UDI
- Description
- Fixative, 2.5 Gallon Cube FDA UDI
Identifiers
- Catalog Number
- 5989 FDA UDI
- Primary DI / UDI-DI
- 00615233080141 FDA UDI
- FDA Product Code
- IFP FDA UDI
- GMDN Term
- 37% Formaldehyde solution IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4010 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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: 37% Formaldehyde solution IVD
Tissue-Tek VIP® 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 1d3227b6-6514-4e1e-a410-54b6d2e438ca 35 fields · synced Jun 6, 2026