Eragon Modular

SHEATH TUBE Ø 10MM SL 447MM Compatible with all ERAGONmodular 10mm inserts in the respective sheath length, along with ERAGONmodular and ERAGONaxial handles without an HF connection,…

Registry build 21.09.26

SHEATH TUBE Ø 10MM SL 447MM Compatible with all ERAGONmodular 10mm inserts in the respective sheath length, along with ERAGONmodular and ERAGONaxial handles without an HF connection, reusable

44manufacturers in China registered for this device type
1catalogue number
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (18), Zhejiang (14), Shanghai (4). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FCL
Manufacturer City Province Registered as Device types
Beijing Zksk Technology Co., Ltd. Beijing Beijing Contract manufacturer 38
Zhejiang Chuangxiang Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Yangzhou Fartley Medical Instrument Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 24
Jiangsu Grit Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 13
Changzhou Jiuhong Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Guangdong MacroLux Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 9
Jiangsu Power-Endo Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 7
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Changshu Rozer Sterilization Technology Co., Ltd. Changshu Jiangsu Contract manufacturer 43
Rozer Sterilization Technology Shuyang Company Limited Shuyang Jiangsu Contract manufacturer 33

Showing 12 of 44. All 44 manufacturers in China registered for Forceps, Biopsy, Non-Electric

Record

Regulatory record for Eragon Modular
Listed by Richard Wolf Gmbh, Germany
FDA product code FCL
Device type Forceps, Biopsy, Non-Electric
Device class Class 1
Regulation 21 CFR 876.1075
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Premarket notification Exempt
Record published 2022-11-01
Record revised 2024-11-21 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Label carries lot or batch number, manufacturing date
Sizes Outer diameter 10 mm; length 447 mm

Catalogue Numbers

Catalogue numbers for Eragon Modular
Catalogue number Size Status
8396902 Outer Diameter 10 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Forceps, Biopsy, Non-Electric Hangzhou AGS MedTech Co., Ltd. 384
Disposable Endoscopic Biopsy Forceps Ningbo Xinwell Medical Technology Co., Ltd. 384
Single Use Biopsy Forceps Zhejiang Chuangxiang Medical Technology Co., Ltd. 224
Surgical Direct Surgical Direct, Inc. 153
Surtex Surtex Instruments Ltd 129
Single-Use Biopsy Forceps Micro-Tech (Nanjing) Co., Ltd. 81
Disposable Biopsy Forceps Olympus Medical Systems Corp. 60
Zksk Beijing Zksk Technology Co., Ltd. 48
Optimos™ Biopsy Forceps Taewoongmedical.co., Ltd. 28
Forceps, Biopsy, Non-Electric Richard Wolf Gmbh 28
Biopsy Forceps Taewoongmedical.co., Ltd. 28
MT Micro-Tech (Nanjing) Co., Ltd. 26

Showing 12 of 117. All products under Forceps, Biopsy, Non-Electric

Recalls

4 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2023-03-24 Class II Under Investigation by firm Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the e 342 units
2023-03-24 Class II Under Investigation by firm Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the e 319 units
2023-03-24 Class II Under Investigation by firm Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the e 280 units
2023-03-24 Class II Under Investigation by firm Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the e 838 units

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