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Perfusor®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Perfusor® FDA UDI
Generic Name
Medicine cabinet FDA UDI
Device Name
SPACE LOCKBOX FOR PERFUSOR SPACE PUMPS FDA UDI
Model / Reference
8713330 FDA UDI
Description
SPACE LOCKBOX FOR PERFUSOR SPACE PUMPS FDA UDI

Identifiers

Catalog Number
8713330 FDA UDI
Primary DI / UDI-DI
04046955083077 FDA UDI
FDA Product Code
MRZ FDA UDI
GMDN Term
Medicine cabinet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Medicine cabinet

Perfusor® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine cabinet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48dba9ae-d710-4d24-861c-887ebb90fded 35 fields · synced Jun 8, 2026