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Easypump

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
EASYPUMP FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
Carry Pouch - Large FDA UDI
Model / Reference
4434455-02 FDA UDI
Description
Carry Pouch - Large FDA UDI

Identifiers

Catalog Number
4434455-02 FDA UDI
Primary DI / UDI-DI
04046964727139 FDA UDI
FDA Product Code
MEB FDA UDI
GMDN Term
Personal device holder, reusable 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

Yes

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

Category: Personal device holder, reusable

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

Similar devices

Also classified as Personal device holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a75dc21f-95d6-4175-a063-b89aa0d4f3ef 35 fields · synced Jun 8, 2026