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Follett

FDA UDI

Class II (US FDA UDI)

by Follett Corporation

Identity

Trade Name
Follett FDA UDI
Generic Name
Blood refrigerator FDA UDI
Device Name
Upright Refrigerator, 20 cu ft, Right hinge and chart recorder FDA UDI
Model / Reference
REF20-BB-R00CR FDA UDI
Description
Upright Refrigerator, 20 cu ft, Right hinge and chart recorder FDA UDI

Identifiers

Catalog Number
00191387 FDA UDI
Primary DI / UDI-DI
00857117006056 FDA UDI
FDA Product Code
KSE FDA UDI
GMDN Term
Blood refrigerator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9700 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Follett by Follett Corporation — Class II — 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

Manufacturer
Follett Corporation

Sources (1)

  • FDA UDI 4c24fab8-9bd2-48ca-8f48-36cdb7f62423 35 fields · synced May 30, 2026