Aesculap

Skin-Graft Ratchet Handle F/BA720R

Registry build 21.09.26
4manufacturers in China registered for this device type
5catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (1), Henan (1), Guangdong (1).

Chinese manufacturers registered for FDA product code FZW
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Henan Huibo Medical Co., Ltd. Nanyang Henan Contract manufacturer 17
Yafho BIO-Technology Co., Ltd. Guangzhou Guangdong Manufacturer 14
Jiangsu MJD Medical Technology Co., Ltd. Taizhou Jiangsu Manufacturer 4

Record

Regulatory record for Aesculap
Listed by Aesculap AG, Germany
FDA product code FZW
Device type Expander, Surgical, Skin Graft
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-05-08
Record revised 2023-01-23 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number

Catalogue Numbers

Catalogue numbers for Aesculap
Catalogue number Size Per pack Status
BA721 10 In distribution
BA723 10 In distribution
BA726R In distribution
BA720R In distribution
BA722 10 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Swann Morton Ltd. Swann Morton, Ltd. 17
Expander, Surgical, Skin Graft Zimmer Orthopaedic Surgical Products 9
Mesh|Ex Exsurco Medical, Inc. 7
Brennen Skin Graft Mesher Stellen Medical, LLC 6
MT Jiangsu MJD Medical Technology Co., Ltd. 4
Meshgraft™ Zimmer Orthopaedic Surgical Products 4
MeshgraftTM II Tissue Expansion System Zimmer Orthopaedic Surgical Products 4
Motiva® Inflatable Balloon Establishment Labs S.A. 3
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 3
4Med 4 MED Ltd. 3
Arthrex® Arthrex, Inc. 3
Dilator KLS-Martin L.P. 2

Showing 12 of 24. All products under Expander, Surgical, Skin Graft

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K936186 1994-03-10

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