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Jackson Biopsy Forceps 1100-710A

by Sontec Instruments, Inc.

Jackson Biopsy Forceps 1100-710A is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00192896082014), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896082014 UDI-DI Date21 Sep 2018ListedStatusListed 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  • Withdrawn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
Jackson Biopsy Forceps
Generic name
Rigid endoscopic biopsy forceps, reusable
Model / Ref / Catalog
1100-710A
Primary DI / UDI-DI
00192896082014
FDA product code
FCL
GMDN term
Rigid endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution
Size
Length — 11.75 Inch

Related devices

Category: Rigid endoscopic biopsy forceps, reusable

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)