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Cryo.s

FDA UDI

Class I (US FDA UDI)

by Greiner Bio-One GmbH

Identity

Trade Name
CRYO.S FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Model / Reference
126273-2D1 FDA UDI

Identifiers

Catalog Number
126273-2D1 FDA UDI
Primary DI / UDI-DI
14039943002010 FDA UDI
FDA Product Code
KDT 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Cryo.s by Greiner Bio-One GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 54f28e5a-6e4e-4ef9-a211-2aa44f4ce4a2 34 fields · synced Jun 8, 2026