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BOSS Instruments 73-1171

by Boss Instruments, Ltd.

BOSS Instruments 73-1171 is a Class II device made by Boss Instruments, Ltd., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00888515179844), 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 Number00888515179844 UDI-DI Date21 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  • Withdrawn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
BOSS Instruments
Generic name
Self-retaining surgical retractor, reusable
Model / Ref / Catalog
73-1171
Primary DI / UDI-DI
00888515179844
FDA product code
GZT
GMDN term
Self-retaining surgical retractor, reusable
Device class
Class II
Regulation number
882.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Self-retaining surgical retractor, reusable

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Other devices filed under Self-retaining surgical retractor, reusable.

Other devices from Boss Instruments, Ltd.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)