RI Syringe

Assisted Reproduction Micromanipulator and Microinjector

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

Concentrated in Guangdong (2), Hubei (1).

Chinese manufacturers registered for FDA product code MQJ
Manufacturer City Province Registered as Device types
Wuhan Huchuang Union Technology Co., Ltd. Wuhan Hubei Manufacturer 8
HUA YUE Medical Technology Co., Ltd. Guangzhou Guangdong Manufacturer 7
Guangzhou Pinzhi Medical Device Co., Ltd. Guangzhou Guangdong Manufacturer 5

Record

Regulatory record for RI Syringe
Listed by Research Instruments Ltd, United Kingdom
FDA product code MQJ
Device type Micromanipulators And Microinjectors, Assisted Reproduction
Device class Class 2
Regulation 21 CFR 884.6150
Establishment Contract manufacturer, Manufacturer
510(k) K003142
Record published 2016-09-17
Record revised 2024-02-28 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for RI Syringe
Catalogue number Size Status
Air Syringe – SAS SE In distribution
Air Syringe – SAS In distribution
Oil Syringe – SOS In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Integra 3 Research Instruments Ltd 22
LifeGlobal® Micropipet LifeGlobal Group, LLC 20
Hariomed HUA YUE Medical Technology Co., Ltd. 4
MTK-1VM-O2 Narishige Lifemed Co., Ltd. 1
SFG Micropipettor Spectrum Fertility Group Inc. 1
MMO-202NDVM Narishige Lifemed Co., Ltd. 1
CellTram® vario Eppendorf AG 1
MTK-1VM-Z3 Narishige Lifemed Co., Ltd. 1
MTK-1VM-O1 Narishige Lifemed Co., Ltd. 1
IM-9CVM Narishige Lifemed Co., Ltd. 1
MTK-1VM-N3 Narishige Lifemed Co., Ltd. 1
MTK-1VM-N4 Narishige Lifemed Co., Ltd. 1

Showing 12 of 42. All products under Micromanipulators And Microinjectors, Assisted Reproduction

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K003142 2000-11-22

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of RI Syringe
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Research Instruments Ltd 510(k) number 2016-03-11 Class II Device Design The units have been fitted with a potentially faulty power supply cable. 380 units 2021-03-02

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