Axiom® MultiPurpose Atraum™ With ClotStop®

Sump Drain, Two Lumens, Silicone, Splittable, With ClotStop®

Registry build 21.09.26
1manufacturer
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code BSO
Manufacturer City Province Registered as Device types
Zhejiang Runqiang Medical Instruments Co., Ltd. Jiaxing Zhejiang Contract manufacturer 9

Record

Regulatory record for Axiom® MultiPurpose Atraum™ With ClotStop®
Listed by Axiom Medical, Inc., United States
FDA product code BSO
Device type Catheter, Conduction, Anesthetic
Device class Class 2
Regulation 21 CFR 868.5120
Establishment Manufacturer
510(k) K993592
Record published 2016-09-24
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Case of 6, box of 10

Catalogue Numbers

Catalogue numbers for Axiom® MultiPurpose Atraum™ With ClotStop®
Catalogue number Size Status
110218AT 18 FR In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 366
Epimed Epimed International, Inc. 56
Avanos Avanos Medical, Inc. 48
E-Cath Tsui Pajunk Gmbh Medizintechnologie 47
Halyard Avanos Medical, Inc. 34
Infiltralong Pajunk Gmbh Medizintechnologie 25
E-Cath acc. Tsui Pajunk Gmbh Medizintechnologie 21
E-Cath Plus acc. Tsui Pajunk Gmbh Medizintechnologie 17
Epinaut Imedicom Co., Ltd. 16
E-Cath® Plus Tsui® Pajunk Gmbh Medizintechnologie 10
E-Cath® II Tsui® Pajunk Gmbh Medizintechnologie 9
Spinaut-E Imedicom Co., Ltd. 9

Showing 12 of 65. All products under Catheter, Conduction, Anesthetic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K993592 2000-05-17
K971851 1998-01-22

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