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Multi-Ad®

FDA UDI

Class I (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
MULTI-AD® FDA UDI
Generic Name
Pharmaceutical fluid-dispensing system FDA UDI
Device Name
MULTI-AD® Transfer Set (MAT4100) FDA UDI
Model / Reference
513548 FDA UDI
Description
MULTI-AD® Transfer Set (MAT4100) FDA UDI

Identifiers

Catalog Number
513548 FDA UDI
Primary DI / UDI-DI
04022495818348 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Pharmaceutical fluid-dispensing system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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: Pharmaceutical fluid-dispensing system

Multi-Ad® by B. Braun Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pharmaceutical fluid-dispensing system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2790ed5c-f09c-47cb-bd24-c0aa9d4263b0 35 fields · synced Jun 8, 2026