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VitriGuard 43842001

by Origio A/S

VitriGuard 43842001 is an assisted reproduction vitrification carrier (FDA Class II; FDA product code MQK, Labware, Assisted Reproduction) made by Origio A/S, listed in FDA GUDID since 3 Oct 2018 (UDI-DI 20888937020414), 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 Number20888937020414 UDI-DI Date3 Oct 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  • Withdrawn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
VitriGuard
Generic name
Assisted reproduction vitrification carrier
Model / reference
43842001
Primary DI / UDI-DI
20888937020414
FDA product code
MQK
GMDN term
Assisted reproduction vitrification carrier
Device class
Class II
Regulation number
884.6160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Assisted reproduction vitrification carrier

Similar devices in this category

Other devices filed under Assisted reproduction vitrification carrier.

Other devices from Origio A/S

See all devices from Origio A/S →

Properties

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