Giftlife™ Fertilization Medium

Giftlife™ Fertilization Medium, 30mL

Registry build 21.09.26
4manufacturers in China registered for this device type
3catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Shandong (1).

Chinese manufacturers registered for FDA product code MQL
Manufacturer City Province Registered as Device types
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Shenzhen VitaVitro Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 7
Gimbo Medical Technology Shenzhen Co., Ltd. Shenzhen Guangdong Manufacturer 3
Shandong Wego Ruisheng Medical Device Co., Ltd. Weihai Shandong Manufacturer 2

Record

Regulatory record for Giftlife™ Fertilization Medium
Listed by Gimbo Medical Technology Shenzhen Co., Ltd., China
FDA product code MQL
Device type Media, Reproductive
Device class Class 2
Regulation 21 CFR 884.6180
Establishment Manufacturer
510(k) K240149
Record published 2024-06-25

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Giftlife™ Fertilization Medium
Catalogue number Size Status
FM30 In distribution
FM60 In distribution
FM10 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LifeGlobal® Media LifeGlobal Group, LLC 93
Sydney IVF William A. Cook Australia PTY, Ltd. 29
LifeGlobal® Media Coopersurgical, Inc. 27
VitaVitro Shenzhen VitaVitro Biotech Co., Ltd. 22
Nidacon Nidacon International AB 19
Sil-Select Plus Lower Layer Fertipro NV 8
FertiCult Mineral Oil Fertipro NV 8
Dewin Donnevie Medical Technology (Shanghai) Co., Ltd. 8
SpermGrad Vitrolife Sweden AB 8
Sequential Culture Media Kitazato Corporation 8
Sperm Wash Medium Invitrocare Inc 7
Enhance-S Plus Vitrolife Inc. 7

Showing 12 of 360. All products under Media, Reproductive

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242043 2025-01-08
K242968 2024-11-22
K240149 2024-06-13
K234023 2024-05-10
K232942 2024-01-30

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer