Identity
- Trade Name
- UNIVERSALCONT.25ML W/SCREW CAP SI FDA UDI
- Generic Name
- Blood/tissue storage/culture container FDA UDI
- Device Name
- UNIVERSALCONT 25ML W/SCREWCAP SI FDA UDI
- Model / Reference
- 364238 FDA UDI
- Description
- UNIVERSALCONT 25ML W/SCREWCAP SI FDA UDI
Identifiers
- Primary DI / UDI-DI
- 15713311000103 FDA UDI
- FDA Product Code
- FMH FDA UDI
- GMDN Term
- Blood/tissue storage/culture container FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3250 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
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
Yes
FDA UDI
Radiation Sterilization FDA UDI
Universalcont.25ml W/Screw Cap Si by Nunc A/S — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nunc A/S
Sources (1)
- FDA UDI a01e67fa-5002-486f-8e8b-1a8e6624e908 34 fields · synced Jun 1, 2026