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0620010104

by Stryker Corp.

0620010104 (620-010-104) is a Class II device made by Stryker Corp., listed in FDA GUDID since 4 Aug 2020 (UDI-DI 07613327163438), 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 Number07613327163438 UDI-DI Date4 Aug 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  • Withdrawn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

Generic name
Laparoscopic insufflator
Model / Ref / Catalog
0620010104, 620-010-104
Primary DI / UDI-DI
07613327163438
FDA product code
HIF
GMDN term
Laparoscopic insufflator
Device class
Class II
Regulation number
884.1730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laparoscopic insufflator

Similar devices in this category

Other devices filed under Laparoscopic insufflator.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

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