Degania

Identi Loops super maxi yellow 18" sterile

Registry build 21.09.26
10manufacturers in China registered for this device type
20catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (3), Zhejiang (2), Guangdong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DXC
Manufacturer City Province Registered as Device types
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Shanghai INT Medical Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 10
Tianjin Demax Medical Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 5
Wickimed (Huizhou) Medical Equipment Manufacturing Co., Ltd. Huizhou Guangdong Contract manufacturer 3
Joykey Industrial (Pinghu) Limited Pinghu Zhejiang Contract manufacturer 43
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Terumo Medical Products (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Beijing Demax Medical Technology Co., Ltd. Beijing Beijing Manufacturer 5

Record

Regulatory record for Degania
Listed by Degania Silicone, Ltd., Israel
FDA product code DXC
Device type Clamp, Vascular
Device class Class 2
Regulation 21 CFR 870.4450
Establishment Contract manufacturer, Specification developer, Manufacturer
Record published 2019-01-09
Record revised 2024-02-23 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Carton of 10, box of 10, shipping carton of 10, 10 of 10

Catalogue Numbers

Catalogue numbers for Degania
Catalogue number Size Status
231021280DS In distribution
231031280DS In distribution
231131280DS In distribution
231051280DS In distribution
231031080DS In distribution
231021080DS In distribution
231221280DS In distribution
231131080DS In distribution
231151080DS In distribution
231141280DS In distribution
231251280DS In distribution
231121280DS In distribution
231041280DS In distribution
231041080DS In distribution
231051080DS In distribution
231151280DS In distribution
231141080DS In distribution
231231280DS In distribution
231121080DS In distribution
231241280DS In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Millennium Avalign Technologies, Inc. 831
Novo Surgical Novo Surgical, Inc. 708
Ambler Surgical Ambler Surgical, LLC 575
Pilling Teleflex Medical LLC 544
Avalign Avalign Technologies, Inc. 543
Boss Instruments Boss Instruments, Ltd. 457
V. Mueller Steris Corporation 432
Wexler Surgical, Inc. Wexler Surgical, Inc. 342
Integra® Jarit® Integra LifeSciences Production Corporation 331
Scanlan® Scanlan International, Inc. 294
HNM Medical HNM Stainless, LLC. 230
Aesculap Aesculap AG 136

Showing 12 of 639. All products under Clamp, Vascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K981956 1998-07-09
K964547 1997-01-08

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