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Norlake

FDA UDI

Class II (US FDA UDI)

by Nor-Lake, Incorporated

Identity

Trade Name
Norlake FDA UDI
Generic Name
Blood refrigerator FDA UDI
Model / Reference
NSBR331WWG/0 FDA UDI

Identifiers

Primary DI / UDI-DI
00851714007065 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
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

Category: Blood refrigerator

Norlake by Nor-Lake, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood refrigerator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 63ea6529-3fd2-4464-a4c4-c2bf8a08ed24 32 fields · synced May 31, 2026