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CryoTube 4, 5 ml SI Internal round

FDA UDI

Class I (US FDA UDI)

by Nunc A/S

Identity

Trade Name
CryoTube 4,5 ml SI Internal round FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
CryoTube 4,5 ml SI Internal round is used for storage and transportation of biological material for in vitro Diagnostics. FDA UDI
Model / Reference
363452 FDA UDI
Description
CryoTube 4,5 ml SI Internal round is used for storage and transportation of biological material for in vitro Diagnostics. FDA UDI

Identifiers

Primary DI / UDI-DI
15713311000172 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

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: General specimen container IVD, no additive/medium

CryoTube 4, 5 ml SI Internal round by Nunc A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nunc A/S

Sources (1)

  • FDA UDI 6fba21af-b5d1-4a63-80d6-8ad0db282e25 33 fields · synced May 30, 2026