Acucise® Procedural Pack Universal Pack B

Kit Contains: B1005, ACUCISE® ENDOPYELOTOMY SYSTEM B3302, STENT, C-FLEX, 7/10F X 28CM B7016, FORTE AxP SET 12/14/18F 35CM 6/BX

Registry build 21.09.26
1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KNY
Manufacturer City Province Registered as Device types
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22

Record

Regulatory record for Acucise® Procedural Pack Universal Pack B
Listed by Applied Medical Resources Corp., United States
FDA product code KNY
Device type Accessories, Catheter, G-U
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
Record published 2015-10-09
Record revised 2024-12-23 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Distribution end date 2018-07-13

Catalogue Numbers

Catalogue numbers for Acucise® Procedural Pack Universal Pack B
Catalogue number Size Status
BK003 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
UroPass Gyrus Acmi, Inc. 15
Ureteral Access Sheath with 2, 3 Fr working channels dilator, 10Frx45cm Promepla 4
Dover Cardinal Health 200, LLC 3
Silhouette® Pediatric Ureteral Stent with Urowire® Guidewire Applied Medical Resources Corp. 3
UroWire® Guidewire with SL-6® Hydrophilic Coating Applied Medical Resources Corp. 2
BI-Flex Access Sheath – 12 inner / 14 outer – Length 45cm Promepla 1
Gyrus Acmi, Inc Gyrus Acmi, Inc. 1
Acucise® Custom KIT Applied Medical Resources Corp. 1
Acucise® Procedural Pack Starter Pack Applied Medical Resources Corp. 1
Bard® “C” Clamp C.R. Bard, Inc. 1
Acucise® Procedural Pack Universal Pack C Applied Medical Resources Corp. 1
Bi-Flex Promepla 1

Showing 12 of 28. All products under Accessories, Catheter, G-U

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K944135 1994-09-21

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