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CryoPRO™-5

FDA UDI

Class II (US FDA UDI)

by Thermogenesis Corp.

Identity

Trade Name
CryoPRO™-5 FDA UDI
Generic Name
Blood cell freeze/thaw system FDA UDI
Device Name
CryoPRO™-5 Cryopreservation/Storage Bag Set FDA UDI
Model / Reference
SGI-0442 FDA UDI
Description
CryoPRO™-5 Cryopreservation/Storage Bag Set FDA UDI

Identifiers

Primary DI / UDI-DI
B039SGI04420 FDA UDI
FDA Product Code
OAO FDA UDI
GMDN Term
Blood cell freeze/thaw system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood cell freeze/thaw system

CryoPRO™-5 by Thermogenesis Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood cell freeze/thaw system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermogenesis Corp.

Sources (1)

  • FDA UDI 05f22a4f-f3dd-4d72-bca3-308352970f4a 35 fields · synced May 30, 2026