Identity
- Trade Name
- Tissue-Tek Genie® CISH FDA UDI
- Generic Name
- Assay container IVD, reusable FDA UDI
- Device Name
- User-Fillable Cartridges for CISH Amplification Linker FDA UDI
- Model / Reference
- 9809-G006 FDA UDI
- Description
- User-Fillable Cartridges for CISH Amplification Linker FDA UDI
Identifiers
- Catalog Number
- 9809-G006 FDA UDI
- Primary DI / UDI-DI
- 00615233010230 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- Assay container IVD, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.1860 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: Assay container IVD, reusable
Tissue-Tek Genie® CISH by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Tissue-Tek Genie® — Sakura Finetek USA, Inc · Class I
- Tissue-Tek® — Sakura Finetek USA, Inc · Class I
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 14a07b5c-991f-45df-9221-884b7fe4540a 35 fields · synced May 30, 2026