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Marketlab Inc 5697

by Marketlab Inc.

Marketlab Inc 5697 is a Class II device made by Marketlab Inc., listed in FDA GUDID since 16 Nov 2018 (UDI-DI 00817517020601), 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 Number00817517020601 UDI-DI Date16 Nov 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  • Withdrawn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
Marketlab Inc
Generic name
Non-fixed blood collection needle
Model / Ref / Catalog
5697
Primary DI / UDI-DI
00817517020601
FDA product code
FMI
GMDN term
Non-fixed blood collection needle
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-fixed blood collection needle

Similar devices in this category

Other devices filed under Non-fixed blood collection needle.

Other devices from Marketlab Inc.

See all devices from Marketlab Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)