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Seamless™ 655409

by B. Braun Medical, Inc.

Seamless™ 655409 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 2 Jul 2017 (UDI-DI 04046964557255), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046964557255 UDI-DI Date2 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • 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  • Withdrawn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
655409
Primary DI / UDI-DI
04046964557255
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

Related devices

Category: Peripheral vascular intervention infusion catheter

Similar devices in this category

Other devices filed under Peripheral vascular intervention infusion catheter.

Other devices from B. Braun Medical, Inc.

See all devices from B. Braun Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)