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CryoTube 1, 8 ml SI Internal thread Round

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 363401

by Nunc A/S

Identity

Trade Name
Nunc™ CryoTube, 1.8mL, sterile, internal thread, round EUDAMED
CryoTube 1,8 ml SI Internal thread Round FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
Nunc™ CryoTube, 1.8mL, sterile, internal thread, round EUDAMED
CryoTube 1,8 ml SI Internal thread Round is used for storage and transportation of biological material for in Vitro Diagnostics. FDA UDI
Model / Reference
363401 EUDAMEDFDA UDI
Description
CryoTube 1,8 ml SI Internal thread Round is used for storage and transportation of biological material for in Vitro Diagnostics. FDA UDI

Identifiers

Primary DI / UDI-DI
15713311000233 EUDAMEDFDA UDI
Basic UDI-DI
B-15713311000233 EUDAMED
FDA Product Code
FMH FDA UDI
EMDN Code
W050299 DEVICES FOR SAMPLES TRANSPORT - OTHER EUDAMED
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: General specimen container IVD, no additive/medium

CryoTube 1, 8 ml SI Internal thread Round by Nunc A/S — Class I — IVDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nunc A/S

Sources (2)

  • FDA UDI 8d8d8a64-cce3-46c7-8be1-50c3e8582668 33 fields · synced Jun 18, 2026
  • EUDAMED 592daee8-4cc5-4fbc-9c7d-8b3578811f0a 61 fields · synced Jun 18, 2026