Jedmed

Adaptor: Olympus Female TO Acmi MAL

Registry build 21.09.26
6manufacturers in China registered for this device type
80catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Jiangsu (1), Anhui (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code EQH
Manufacturer City Province Registered as Device types
Beijing Fanxing Guangdian Medical Treatment Equipment Co Ltd Beijing Beijing Contract manufacturer 5
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Shenzhen Eyco Technology Co., Ltd. Shenzhen Guangdong Manufacturer 27
Anhui Shiyin Photoelectric Instrument Co., Ltd. Suzhou Anhui Specification developer 18
Guangzhou T.K Medical Instrument Co., Ltd. Guangzhou Guangdong Contract manufacturer 7
Shenzhen Shanglaite Electronic Technology Co., Ltd. Shenzhen Guangdong Remanufacturer 4

Record

Regulatory record for Jedmed
Listed by Jedmed Instrument Company, United States
FDA product code EQH
Device type Source, Carrier, Fiberoptic Light
Device class Class 1
Regulation 21 CFR 874.4350
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2023-02-03
Record revised 2026-05-18 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Jedmed
Catalogue number Size Status
99-7840 In distribution
99-7825 In distribution
99-7749 In distribution
99-7709 In distribution
99-7707 In distribution
99-7935 In distribution
99-7995 In distribution
99-7800 In distribution
99-7747 In distribution
99-7867 In distribution
99-8202 In distribution
42-8157-3 In distribution
99-7741 In distribution
99-7859 In distribution
99-8016 In distribution
99-8060 In distribution
99-7850 In distribution
99-7820 In distribution
99-7975 In distribution
99-8200 In distribution
99-8204 In distribution
99-7742 In distribution
99-7862 In distribution
99-7830 In distribution
99-8082 In distribution
99-7810 In distribution
99-7991 In distribution
99-7740 In distribution
42-8157-1 In distribution
99-7708 In distribution
99-8058 In distribution
99-7861-1 In distribution
42-8157-2 In distribution
99-7868 In distribution
42-8167-2 In distribution
99-8050 In distribution
99-7746-1 In distribution
99-7745 In distribution
99-7866 In distribution
99-7710 In distribution
99-8057 In distribution
99-8078 In distribution
99-7940 In distribution
99-8000 In distribution
99-7992 In distribution
99-8056 In distribution
99-8074 In distribution
99-7743 In distribution
99-8070 In distribution
99-7863-1 In distribution
99-7994 In distribution
99-7990 In distribution
99-8056-10 In distribution
42-8167-1 In distribution
99-7746 In distribution
99-7870 In distribution
99-7830-1 In distribution
99-8073 In distribution
99-8086 In distribution
99-8015 In distribution
42-8167-3 In distribution
99-8084 In distribution
99-7830-2 In distribution
99-7750 In distribution
99-7993 In distribution
99-8075 In distribution
99-8076 In distribution
99-8091 In distribution
99-7980 In distribution
99-7942 In distribution
99-7712 In distribution
99-7860 In distribution
99-8206 In distribution
99-8062 In distribution
99-7711 In distribution
99-7875-5 In distribution
99-7748 In distribution
99-8055 In distribution
99-8072 In distribution
99-7875 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pilling Teleflex Medical LLC 216
Millennium Avalign Technologies, Inc. 72
Ambler Surgical Ambler Surgical, LLC 40
Elmed Incorporated Elmed, Inc. 36
Fentex Fentex medical GmbH 36
MicroFrance® Integra Microfrance SAS 24
Elmed Elmed, Inc. 23
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 19
Source, Carrier, Fiberoptic Light Schölly Fiberoptic GmbH 17
BR Surgical, LLC BR Surgical LLC 16
Bear Mytamed, Inc. 12
mytaMed Mytamed, Inc. 12

Showing 12 of 50. All products under Source, Carrier, Fiberoptic Light

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K954184 1995-11-13
K912885 1991-08-30
K896384 1990-01-23

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