SapphireTM

SDS-1 Sapphire Detachment SYS

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
11510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (2), Guangdong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HCG
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Microport Neurotech (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 2

Record

Regulatory record for SapphireTM
Listed by Micro Therapeutics, Inc., United States
FDA product code HCG
Device type Device, Neurovascular Embolization
Device class Class 2
Regulation 21 CFR 882.5950
510(k) K030392
Record published 2016-10-02
Record revised 2023-05-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Storage Special storage condition: Store in a clean, dry and secure location

Catalogue Numbers

Catalogue numbers for SapphireTM
Catalogue number Size Status
SDS-1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Optima Coil System Balt USA, LLC 307
Penumbra Coil 400 Penumbra Inc. 268
Smart Coil Penumbra Inc. 238
Axium™ Detachable Coil System Micro Therapeutics, Inc. 234
Numen Microport Neurotech (Shanghai) Co., Ltd. 223
Axium™ Prime Detachable Coil System Micro Therapeutics, Inc. 141
Barricade Coil System Balt USA, LLC 137
Numen Helia Microport Neurotech (Shanghai) Co., Ltd. 129
V-Trak MicroVention, Inc. 106
HydroSoft Helical MicroVention, Inc. 94
AxiumTM Micro Therapeutics, Inc. 89
LP Coil System Penumbra Inc. 77

Showing 12 of 99. All products under Device, Neurovascular Embolization

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060747 2007-04-24
K060625 2006-04-20
K051560 2005-06-28
K051425 2005-06-22
K050543 2005-04-27
K041649 2004-07-16
K040694 2004-03-25
K033372 2004-01-09
K032497 2003-09-25
K031852 2003-08-20
K030392 2003-07-21

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