Device Explorer · FDA GUDID · GMDN 44046

IVF medium

A solution that provides a physiological environment for the retrieval, culture, maintenance, transfer, and/or storage of human sperm, harvested oocytes (eggs), and/or resulting embryos associated with the method of in vitro fertilization (IVF). The solution t

US‑registered devices552in commercial distribution
Companies19labelers on GUDID
Single‑use40%of device records
Sterile100%labelled sterile
Prescription83%Rx‑only share
ShareLinkedIn

Share of device records

Coopersurgical, Inc.10820%
Origio A/S5911%
Lifeglobal Group, Llc499%
Fujifilm Irvine Scientific, Inc.438%
Irvine Scientific, Llc438%
Vitrolife Sweden Ab336%
Fertipro Nv316%
Invitrocare, Incorporated316%

Top labelers

CompanyDevicesShare
Coopersurgical, Inc.10820%
Origio A/S5911%
Lifeglobal Group, Llc499%
Fujifilm Irvine Scientific, Inc.438%
Irvine Scientific, Llc438%
Vitrolife Sweden Ab336%
Fertipro Nv316%
Invitrocare, Incorporated316%
Kitazato Corporation275%
Gimbo Medical Technology Shenzhen Co., Ltd.244%
Shenzhen Vitavitro Biotech Co.,Ltd.234%
Vitromed Gmbh193%

Company = labeler of record on GUDID. 19 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CaseBioscience®SpermGradG-MOPS PLUSG-MOPSASPG-RINSEGx-MOPS PLUSGx-TLGx-IVFG-IVF PLUSG-2 PLUSG-1 PLUSG-TLSpermRinseOVOILOVOIL HEAVY

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

FDA product codes

CodeNameDevices
MQLMedia, Reproductive482
MQLMEDIA, REPRODUCTIVE130
QKIMedia, Reproductive, Exempt21
QKIMedia, reproductive, exempt12
HDRCap, Cervical4
MTWSystem,Water,Reproduction,Assisted,And Purification2

GMDN & GCC registration

  • GMDN code 44046 · non‑implantable
  • Single‑use 40% · sterile 100% · Rx‑only 83% · 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

Total Volume (Milliliter) · 123Total Volume (Liter) · 2

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No closely related category with 50+ devices.

How many ivf medium products are registered in the US?

552 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "IVF medium", from 19 companies. The largest labeler is Coopersurgical, Inc. with 20% of records.

Which FDA product codes apply?

MQL (Media, Reproductive), MQL (MEDIA, REPRODUCTIVE), QKI (Media, Reproductive, Exempt), QKI (Media, reproductive, exempt)

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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