Skip to content

Kitazato Blastomere Biopsy Micropipette MT-BPBM-20-35

by Kitazato Corporation

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04573316388927 UDI-DI Date7 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Kitazato Blastomere Biopsy Micropipette
Generic Name
Assisted reproduction microtool
Model / Ref / Catalog
MT-BPBM-20-35, 95349
Primary DI / UDI-DI
04573316388927
FDA Product Code
PUC
GMDN Term
Assisted reproduction microtool
Device Class
Class II
Regulation Number
884.6130
GUDID distribution status
In Commercial Distribution

Other devices from Kitazato Corporation

See all devices from Kitazato Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No