Skip to content

Kitazato ET Catheter Type2-v5 EC-PRO Supported 205118 Type2-v5 EC-PRO Supported

by Kitazato Corporation

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number04580303269589 UDI-DI Date7 Feb 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Kitazato ET Catheter Type2-v5 EC-PRO Supported
Generic Name
Assisted reproduction transfer catheter/set
Model / Ref / Catalog
205118 Type2-v5 EC-PRO Supported, 205118
Primary DI / UDI-DI
04580303269589
510(k) Number
FDA Product Code
MQF
GMDN Term
Assisted reproduction transfer catheter/set
Device Class
Class II
Regulation Number
884.6110
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K162878)

Show all (12)

Other devices from Kitazato Corporation

See all devices from Kitazato Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (8)

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