GEL-Bead

4 catalogue numbers from IPN001485, listed by Teleflex Medical LLC, United States, under Device, Vascular, For Promoting Embolization. 6 manufacturers in China are registered for this product code.

Registry build 21.09.26
6manufacturers in China registered for this device type
4catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (1), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRD
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Microport Neurotech (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 2
Suzhou Haowei Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 1

Record

Regulatory record for GEL-Bead
Listed by Teleflex Medical LLC, United States
FDA product code KRD
Device type Device, Vascular, For Promoting Embolization
Device class Class 2
Regulation 21 CFR 870.3300
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2020-04-23
Record revised 2024-01-22 (version 3)

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
Label carries lot or batch number
Packaging Pack of 5, box of 5

Catalogue Numbers

Catalogue numbers for GEL-Bead
Catalogue number Size Status
IPN001485 700-1000 Micrometer Sphere Size In distribution
IPN001479 100-300 Micrometer Sphere Size In distribution
IPN001481 300-500 Micrometer Sphere Size In distribution
IPN001483 500-700 Micrometer Sphere Size In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prestige Coil System Balt USA, LLC 339
Axium™ Detachable Coil System Micro Therapeutics, Inc. 279
Optima Coil System Balt USA, LLC 255
AxiumTM Micro Therapeutics, Inc. 255
Avenir Shanghai Wallaby Medical Technologies Co., Inc. 184
MReye Cook Incorporated 167
Axium™ Prime Detachable Coil System Micro Therapeutics, Inc. 162
Nester Cook Incorporated 160
Axium Micro Therapeutics, Inc. 146
ConcertoTM Micro Therapeutics, Inc. 133
Tornado Cook Incorporated 111
V-Trak MicroVention, Inc. 105

Showing 12 of 158. All products under Device, Vascular, For Promoting Embolization

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P780011 1988-01-29 MINI BALLOON Bd Becton Dickinson Vacutainer Systems Preanalytic

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