Bead Block™

Catalogue number EB2S507-US, listed by Boston Scientific Corporation, United States, under Agents, Embolic, For Treatment Of Uterine Fibroids. 1 manufacturer in China is registered for this product code.

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

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code NAJ
Manufacturer City Province Registered as Device types
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Bead Block™
Listed by Boston Scientific Corporation, United States
FDA product code NAJ
Device type Agents, Embolic, For Treatment Of Uterine Fibroids
Device class Class 2
Regulation 21 CFR 870.3300
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2021-10-14

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Bead Block™
Catalogue number Size Status
EB2S507-US In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Embosphere® Biosphere Medical, Inc. 24
Embozene Microspheres (Opaque) Celonova Biosciences, Inc. 20
Embozene Microspheres (Color-Advanced) Celonova Biosciences, Inc. 20
Contour™ Boston Scientific Corporation 14
HydroPearl MicroVention, Inc. 12
Bearing nsPVA® Merit Medical Systems, Inc. 7
Cook Cook Incorporated 2
Embozene Color Advance 700um Embozene 1mL Colored – US Varian Medical Systems, Inc 1
Embozene Color Advance 900um Embozene 1mL Colored – US Varian Medical Systems, Inc 1
Embozene Color Advance 500um Embozene 2mL Colored – US Varian Medical Systems, Inc 1
Embozene Color Advance 250um Embozene 2mL Colored – US Varian Medical Systems, Inc 1
Embozene Color Advance 250um Embozene 1mL Colored – US Varian Medical Systems, Inc 1

Showing 12 of 18. All products under Agents, Embolic, For Treatment Of Uterine Fibroids

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K100663 2010-04-16
K030966 2003-09-23

Recalls

The FDA has not published a severity grade for these. 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 Closed
2009-08-17 Not classified Process design Compromised sterility: Boston Scientific is initiating a Recall Removal for twenty (20) UPN codes and 638 associated lots/batches of its Contour SE Microspheres product. All affected product is packaged within a vial. Boston Scientific h 45,724 (13,048 US, 45,724 OUS) 2011-12-18

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