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Device Explorer · FDA GUDID · GMDN 46870

Intrauterine scoop

A heavy, hand-held, manual surgical instrument with a spoon-like, sharp-edged distal end on a long shaft that is used to access and scrape (gouge or scoop out) a particular area of the lining of the uterus for its removal during a gynaecological procedure. The

US‑registered devices63in commercial distribution
Companies2labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription17%Rx‑only share
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Share of device records

Hnm Stainless, Llc.5283%
Medicon Eg. Chirurgiemechaniker-Genossenschaft1117%

Top labelers

CompanyDevicesShare
Hnm Stainless, Llc.5283%
Medicon Eg. Chirurgiemechaniker-Genossenschaft1117%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MediconHNM MedicalHNM MEDICAL

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
FZSCurette, Surgical, General Use41
MDMInstrument, Manual, Surgical, General Use12
HCYCURETTE, UTERINE10
FZSCURETTE, SURGICAL, GENERAL USE1

GMDN & GCC registration

  • GMDN code 46870 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 17% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many intrauterine scoop products are registered in the US?

63 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intrauterine scoop", from 2 companies. The largest labeler is Hnm Stainless, Llc. with 83% of records.

Which FDA product codes apply?

FZS (Curette, Surgical, General Use), MDM (Instrument, Manual, Surgical, General Use), HCY (CURETTE, UTERINE), FZS (CURETTE, SURGICAL, GENERAL USE)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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