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FSSB Nylon Suture 9000AE

by Fssb Chirurgische Nadeln GmbH

FSSB Nylon Suture 9000AE is a Class II device made by Fssb Chirurgische Nadeln GmbH, listed in FDA GUDID since 21 Sep 2016 (UDI-DI EFSB9000AE2), 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 NumberEFSB9000AE2 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
FSSB Nylon Suture
Generic name
Nylon suture, non-bioabsorbable, monofilament
Model / reference
9000AE
Primary DI / UDI-DI
EFSB9000AE2
FDA product code
GAR
GMDN term
Nylon suture, non-bioabsorbable, monofilament
Device class
Class II
Regulation number
878.5020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nylon suture, non-bioabsorbable, monofilament

Similar devices in this category

Other devices filed under Nylon suture, non-bioabsorbable, monofilament.

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Properties

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