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Premilene B2090454

by B Braun Surgical SA

Premilene B2090454 is a Class II device made by B Braun Surgical SA, listed in FDA GUDID since 5 Aug 2015 (UDI-DI 04046964115912), 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 Number04046964115912 UDI-DI Date5 Aug 2015ListedStatusListed 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  • Withdrawn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
Premilene
Generic name
Polyolefin/fluoropolymer suture, monofilament
Model / Ref / Catalog
B2090454
Primary DI / UDI-DI
04046964115912
FDA product code
GAW
GMDN term
Polyolefin/fluoropolymer suture, monofilament
Device class
Class II
Regulation number
878.5010
GUDID distribution status
In Commercial Distribution
Size
Length — 100.00 Centimeter

Related devices

Category: Polyolefin/fluoropolymer suture, monofilament

Similar devices in this category

Other devices filed under Polyolefin/fluoropolymer suture, monofilament.

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)