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HEMOVAULT by ACCUCOLD

FDA UDI

Class II (US FDA UDI)

by Felix Storch, Inc.

Identity

Trade Name
HEMOVAULT by ACCUCOLD FDA UDI
Generic Name
Blood refrigerator FDA UDI
Device Name
25 Cu. Ft. Glass Door Pharmaceutical / Laboratory High Performance Blood Bank Stainless Steel Refrigerator FDA UDI
Model / Reference
AHBBG254SS FDA UDI
Description
25 Cu. Ft. Glass Door Pharmaceutical / Laboratory High Performance Blood Bank Stainless Steel Refrigerator FDA UDI

Identifiers

Catalog Number
AHBBG254SS FDA UDI
Primary DI / UDI-DI
00761101151793 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood refrigerator

HEMOVAULT by ACCUCOLD by Felix Storch, Inc. — 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

Manufacturer
Felix Storch, Inc.

Sources (1)

  • FDA UDI 01c30787-e9df-4370-9b92-81e665d17b57 35 fields · synced Jun 8, 2026