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Connector

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Connector FDA UDI
Generic Name
Luer/Luer linear connector, single-use FDA UDI
Device Name
DMA 1000 Dual Male Adapter FDA UDI
Model / Reference
456080 FDA UDI
Description
DMA 1000 Dual Male Adapter FDA UDI

Identifiers

Catalog Number
456080 FDA UDI
Primary DI / UDI-DI
04046964183669 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Luer/Luer linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer/Luer linear connector, single-use

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

Similar devices

Also classified as Luer/Luer linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa826402-d1bf-4a9f-abd2-458ebeeed5a0 35 fields · synced Jun 8, 2026