Skip to content

gSource gS 49.8700

by Gsource, LLC.

gSource gS 49.8700 is a Class I device made by Gsource, LLC., listed in FDA GUDID since 3 Jan 2020 (UDI-DI 00840314223500), 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 Number00840314223500 UDI-DI Date3 Jan 2020ListedStatusListed 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  • Withdrawn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
gSource
Generic name
Scalpel, reusable
Model / Ref / Catalog
gS 49.8700
Primary DI / UDI-DI
00840314223500
FDA product code
HTS
GMDN term
Scalpel, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Scalpel, reusable

Similar devices in this category

Other devices filed under Scalpel, reusable.

Other devices from Gsource, LLC.

See all devices from Gsource, LLC. →

Properties

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