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Instrapac 7958

by Robinson Healthcare Limited

Instrapac 7958 is an uterine sound (FDA Class I; FDA product code HHM, Sound, Uterine) made by Robinson Healthcare Limited, listed in FDA GUDID since 21 May 2025 (UDI-DI 05010058079588), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05010058079588 UDI-DI Date21 May 2025ListedStatusListed 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  • Withdrawn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
Instrapac
Generic name
Uterine sound, single-use
Model / Ref / Catalog
7958
Primary DI / UDI-DI
05010058079588
FDA product code
HHM
GMDN term
Uterine sound, single-use
Device class
Class I
Regulation number
884.4530
GUDID distribution status
In Commercial Distribution
Size
Length — 32 Centimeter

Related devices

Category: Uterine sound, single-use

Similar devices

Other devices filed under FDA product code HHM (Sound, Uterine).

Other devices from Robinson Healthcare Limited

See all devices from Robinson Healthcare Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)