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Micro Friedman Rongeur 1106-076

by Sontec Instruments, Inc.

Micro Friedman Rongeur 1106-076 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00192896083332), 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 Number00192896083332 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  • Withdrawn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
Micro Friedman Rongeur
Generic name
Orthopaedic joint/limb rongeur
Model / Ref / Catalog
1106-076
Primary DI / UDI-DI
00192896083332
FDA product code
HTX
GMDN term
Orthopaedic joint/limb rongeur
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Size
Length — 5.5 Inch

Related devices

Category: Orthopaedic joint/limb rongeur

Similar devices in this category

Other devices filed under Orthopaedic joint/limb rongeur.

Other devices from Sontec Instruments, Inc.

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Properties

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