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Device Explorer · FDA GUDID · GMDN 56648

Assisted reproduction procedure dish

A container intended exclusively for preparing and culturing gametes or embryos for use in assisted reproduction techniques (ART). Such techniques include in vitro fertilization (IVF), fertilization via intracytoplasmic sperm injection (ICSI), or other in IVF

US‑registered devices86in commercial distribution
Companies16labelers on GUDID
Single‑use92%of device records
Sterile99%labelled sterile
Prescription43%Rx‑only share
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Share of device records

Wuhan Huchuang Union Technology Co., Ltd.1416%
Shenzhen Vitavitro Biotech Co.,Ltd.1214%
Spectrum Fertility Group Inc.910%
Astec Co.,Ltd.78%
Coopersurgical, Inc.78%
Lifeglobal Group, Llc78%
Vitrolife Sweden Ab78%
Corning Incorporated56%

Top labelers

CompanyDevicesShare
Wuhan Huchuang Union Technology Co., Ltd.1416%
Shenzhen Vitavitro Biotech Co.,Ltd.1214%
Spectrum Fertility Group Inc.910%
Astec Co.,Ltd.78%
Coopersurgical, Inc.78%
Lifeglobal Group, Llc78%
Vitrolife Sweden Ab78%
Corning Incorporated56%
Nunc A/S56%
Vitrolife A/S33%
Invo Bioscience, Inc.33%
Nalge Nunc International Corporation22%

Company = labeler of record on GUDID. 16 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MetiecHariomed culture dishVitaVitroEmbryoSlide+ culture dishEmbryoSlide culture dishEmbryoSlide+ ic8 dishReproPlateEmbryo GridLifeGlobal® GPS® DishwareNunc IVF ICSI DishNunc IVF Center Well DishINVOcell Retention DeviceINVOcell Culture DeviceSwimCount® HarvesterICSI DishCentre Well Dish

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

FDA product codes

CodeNameDevices
PUDLabware, Assisted Reproduction, Exempt55
MQKLABWARE, ASSISTED REPRODUCTION16
MQKLabware, Assisted Reproduction15
OYOCulture, Intravaginal, Assisted Reproduction6
MQGAccessory, Assisted Reproduction3
PUDLabware, assisted reproduction, exempt2

GMDN & GCC registration

  • GMDN code 56648 · non‑implantable
  • Single‑use 92% · sterile 99% · Rx‑only 43% · 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 assisted reproduction procedure dish products are registered in the US?

86 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Assisted reproduction procedure dish", from 16 companies. The largest labeler is Wuhan Huchuang Union Technology Co., Ltd. with 16% of records.

Which FDA product codes apply?

PUD (Labware, Assisted Reproduction, Exempt), MQK (LABWARE, ASSISTED REPRODUCTION), MQK (Labware, Assisted Reproduction), OYO (Culture, Intravaginal, Assisted Reproduction)

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.

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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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