Identity
- Trade Name
- Water for Injection, USP Sterile Grade FDA UDI
- Generic Name
- Ex vivo cell culture medium FDA UDI
- Model / Reference
- 04 FDA UDI
Identifiers
- Catalog Number
- WFI-USP-2XL FDA UDI
- Primary DI / UDI-DI
- B891WFIUSP2XL0 FDA UDI
- FDA Product Code
- KIT FDA UDI
- GMDN Term
- Ex vivo cell culture medium 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ex vivo cell culture medium
Water for Injection, USP Sterile Grade by Intermountain Life Sciences, Llc — 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
- Intermountain Life Sciences, Llc
Sources (1)
- FDA UDI 0f9f54e3-07df-42ac-8c27-aa1daa1c0b21 34 fields · synced May 30, 2026