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Milex MXKPERK09

by CooperSurgical, Inc.

Milex MXKPERK09 is a Class II device made by CooperSurgical, Inc., listed in FDA GUDID since 28 Jul 2016 (UDI-DI 60888937006430), 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 Number60888937006430 UDI-DI Date28 Jul 2016ListedStatusListed 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  • Withdrawn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
Milex
Generic name
Pelvic-organ-supporting pessary
Model / reference
MXKPERK09
Primary DI / UDI-DI
60888937006430
FDA product code
HHW
GMDN term
Pelvic-organ-supporting pessary
Device class
Class II
Regulation number
884.3575
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pelvic-organ-supporting pessary

Similar devices

Other devices filed under FDA product code HHW (Pessary, Vaginal).

Other devices from CooperSurgical, Inc.

See all devices from CooperSurgical, Inc. →

Properties

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