Identity
- Trade Name
- Eos-TIC 1:32 FDA UDI
- Generic Name
- Granulocyte IVD, reagent FDA UDI
- Model / Reference
- 004019-6010 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04061609000286 FDA UDI
- FDA Product Code
- JCG FDA UDI
- GMDN Term
- Granulocyte IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.8200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Category: Granulocyte IVD, reagent
Eos-TIC 1:32 by BIOANALYTIC GmbH, biomed. Analysentechnik — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Granulocyte IVD, reagent.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BIOANALYTIC GmbH, biomed. Analysentechnik
Sources (1)
- FDA UDI a2dd3c45-4b06-456e-978d-b3179c99ba95 32 fields · synced May 30, 2026