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FibriJet SA-6111

by Micromedics, Inc.

FibriJet SA-6111 is an open-surgery adhesive/sealant applicator (FDA Class II; FDA product code FMF, Syringe, Piston) made by Micromedics, Inc., listed in FDA GUDID since 25 Sep 2016 (UDI-DI 00815634020320), 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 Number00815634020320 UDI-DI Date25 Sep 2016ListedStatusListed 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  • Withdrawn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
FibriJet
Generic name
Open-surgery adhesive/sealant applicator, dual-channel
Model / reference
SA-6111
Primary DI / UDI-DI
00815634020320
FDA product code
FMF
GMDN term
Open-surgery adhesive/sealant applicator, dual-channel
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Open-surgery adhesive/sealant applicator, dual-channel

Similar devices in this category

Other devices filed under Open-surgery adhesive/sealant applicator, dual-channel.

Other devices from Micromedics, Inc.

See all devices from Micromedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)