Seamless™ 655412

by B. Braun Medical, Inc.

Seamless™ 655412 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04046964557293), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04046964557293 UDI-DI	Date24 Sep 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04046964557293

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Seamless™
Generic name: Peripheral vascular intervention infusion catheter
Model / Ref / Catalog: 655412

Primary DI / UDI-DI: 04046964557293
FDA product code: OFL
GMDN term: Peripheral vascular intervention infusion catheter

Device class: Class II
Regulation number: 870.1340
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)