← Back to catalogue
Nunc™ Universal™ Tube, 2 mL internally-threaded, Racked
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Nunc™ Universal™ Tube, 2 mL internally-threaded, Racked FDA UDI
- Generic Name
- General specimen container IVD, no additive/medium FDA UDI
- Device Name
- 2.0ML INT 2D WP GRADS UNILATCH FDA UDI
- Model / Reference
- 374510 FDA UDI
- Description
- 2.0ML INT 2D WP GRADS UNILATCH FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850016058550 FDA UDI
- FDA Product Code
- FMH FDA UDI
- GMDN Term
- General specimen container IVD, no additive/medium 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
No
FDA UDI
Radiation Sterilization FDA UDI
Nunc™ Universal™ Tube, 2 mL internally-threaded, Racked by Nalge Nunc International Corporation — Class I — FDA UDI — listed in FDA GUDID
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
- Nalge Nunc International Corporation
Sources (1)
- FDA UDI b1165df3-da82-4537-9946-1b85dc100c9d 34 fields · synced Jun 9, 2026