← Back to catalogue

Nalgene™ Cryogenic Tube, 1.2 mL externally-threaded

FDA UDI

Class I (US FDA UDI)

by Nalge Nunc International Corporation

Identity

Trade Name
Nalgene™ Cryogenic Tube, 1.2 mL externally-threaded FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
BLK STRL CRYOGNCVL PP; 1.2ML FDA UDI
Model / Reference
5012-0012 FDA UDI
Description
BLK STRL CRYOGNCVL PP; 1.2ML FDA UDI

Identifiers

Primary DI / UDI-DI
10850016058680 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
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
Sterilization Method
Radiation Sterilization FDA UDI

Category: General specimen container IVD, no additive/medium

Nalgene™ Cryogenic Tube, 1.2 mL externally-threaded by Nalge Nunc International Corporation — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nalge Nunc International Corporation

Sources (1)

  • FDA UDI 2f145265-a09e-4d08-8842-609d605a2fa4 34 fields · synced Jun 9, 2026