Identity
- Trade Name
- DHI Media & Controls FDA UDI
- Generic Name
- Cell culture medium IVD FDA UDI
- Device Name
- SUPPL FOR 10-200100 EU2 PLT MD FDA UDI
- Model / Reference
- 10-200100EU1 FDA UDI
- Description
- SUPPL FOR 10-200100 EU2 PLT MD FDA UDI
Identifiers
- Catalog Number
- 10-200100EU1 FDA UDI
- Primary DI / UDI-DI
- 30014613331162 FDA UDI
- FDA Product Code
- KIT FDA UDI
- GMDN Term
- Cell culture medium IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.2220 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
Yes
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: Cell culture medium IVD
DHI Media & Controls by Diagnostic Hybrids, 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
- Diagnostic Hybrids, Inc.
Sources (1)
- FDA UDI ec0fd696-0a3a-4c0a-8b14-9f39d663f5bd 35 fields · synced Jun 1, 2026