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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
Bedside syringe pump FDA UDI
Device Name
Perfusor® Space® Syringe Pump, Non-Wireless FDA UDI
Model / Reference
8713032U FDA UDI
Description
Perfusor® Space® Syringe Pump, Non-Wireless FDA UDI

Identifiers

Catalog Number
8713032U FDA UDI
Primary DI / UDI-DI
04046964797965 FDA UDI
FDA Product Code
LZH FDA UDI
FRN FDA UDI
GMDN Term
Bedside syringe pump 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bedside syringe pump

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

Similar devices

Also classified as Bedside syringe pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI e6c03b49-9517-4469-a5ed-8198d9f96028 36 fields · synced Jun 1, 2026