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B.braun

FDA UDI

Class U (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
B.BRAUN FDA UDI
Generic Name
Tissue expander injection port FDA UDI
Device Name
BBRAUN MEDICAL 21G X 4.4CM WINGED INF FDA UDI
Model / Reference
7B3050 FDA UDI
Description
BBRAUN MEDICAL 21G X 4.4CM WINGED INF FDA UDI

Identifiers

Catalog Number
7B3050 FDA UDI
Primary DI / UDI-DI
04046964341298 FDA UDI
FDA Product Code
LCJ FDA UDI
GMDN Term
Tissue expander injection port FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue expander injection port

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

Similar devices

Also classified as Tissue expander injection port.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59d0614c-0dbf-49e3-910d-6c53819edf50 35 fields · synced May 29, 2026