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Sims Curette 392-113

by CooperSurgical, Inc.

Sims Curette 392-113 is a Class I device made by CooperSurgical, Inc., listed in FDA GUDID since 30 Oct 2022 (UDI-DI 00888937017441), 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 Number00888937017441 UDI-DI Date30 Oct 2022ListedStatusListed 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  • Withdrawn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
Sims Curette
Generic name
Endometrial biopsy curette
Model / reference
392-113
Description
Sims Curette, size 3: 11 mm
Primary DI / UDI-DI
00888937017441
FDA product code
FZS
GMDN term
Endometrial biopsy curette
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 11 Millimeter

Related devices

Category: Endometrial biopsy curette

Similar devices in this category

Other devices filed under Endometrial biopsy curette.

Other devices from CooperSurgical, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)