Reli®

Reli Gem Safety Blood Collection Set 21G x 3/4", 12" tubing with EZ Flash Technology

Registry build 21.09.26
49manufacturers in China registered for this device type
28catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (12), Jiangsu (11), Shanghai (10). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FPA
Manufacturer City Province Registered as Device types
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Hantech Medical Device Co., Ltd. Cixi Zhejiang Contract manufacturer 18
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
BQ Plus Medical Co., Ltd. Songjiang Shanghai Contract manufacturer 13
Ningbo Tianyi Medical Appliance Co., Ltd. Ningbo Zhejiang Contract manufacturer 11
Anhui Tiankang Medical Technology Co., Ltd. Tianchang Anhui Contract manufacturer 9
Anhui Kangda Medical Products Co., Ltd. Tianchang Anhui Contract manufacturer 7
JDI Electronics Factory Dongguan Guangdong Contract manufacturer 7
Yangzhou Xingwei Medical Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 5
Wenzhou K.L.F. Medical Plastics Co., Ltd. Wenzhou Zhejiang Contract manufacturer 4
Advance Technology Ltd Shenzhen Guangdong Contract manufacturer 3
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3

Showing 12 of 49. All 49 manufacturers in China registered for Set, Administration, Intravascular

Record

Regulatory record for Reli®
Listed by Myco Medical Supplies, Inc., United States
FDA product code FPA
Device type Set, Administration, Intravascular
Device class Class 2
Regulation 21 CFR 880.5440
510(k) K170276
Record published 2024-02-22
Record revised 2021-04-07 (version 2)

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
Packaging Inner carton of 100, case of 9, case of 8, inner carton of 50
Sizes Needle gauge 21 to 25 G

Catalogue Numbers

Catalogue numbers for Reli®
Catalogue number Size Status
GSBCS21G-12 Needle Gauge 21 G In distribution
GSBCS21G-7 7″ tubing In distribution
GSIS25G-12 12″ tubing In distribution
GSBCS23G-12 12″ tubing In distribution
GSBCS25G-12 12″ tubing In distribution
GSIS25G-3 3″ tubing In distribution
GSBCS25G-12T 12″ tubing In distribution
GSBCS25G-7 7″ tubing In distribution
GSBCS23G-3 3″ tubing In distribution
GSBCS25G-3T 3″ tubing In distribution
GSBCS21G-3T 3″ tubing In distribution
GSBCS23G-7T 7″ tubing In distribution
GSBCS23G-3T 3″ tubing In distribution
GSIS23G-12 12″ tubing In distribution
GSBCS25G-7T 7″ tubing In distribution
GSBCS21G-3 3″ tubing In distribution
GSBCS21G-12T 12″ tubing In distribution
GSIS25G-7 7″ tubing In distribution
GSIS21G-7 Needle Gauge 21 G In distribution
GSIS21G-12 12″ tubing In distribution
GSBCS25G-3 3″ tubing In distribution
GSBCS21G-12 12″ tubing In distribution
GSIS23G-7 7″ tubing In distribution
GSIS23G-3 3″ tubing In distribution
GSBCS23G-12T 12″ tubing In distribution
GSIS21G-3 3″ tubing In distribution
GSBCS21G-7T 7″ tubing In distribution
GSBCS23G-7 7″ tubing In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ICU Medical ICU Medical, Inc 529
Codan Codan US Corp. 510
Vygon Vygon Corp. 355
Port Access Needle Bard Access Systems, Inc. 341
Set, Administration, Intravascular Mps Medical, Inc. 291
Alaris, SmartSite BD Switzerland Sàrl 266
IV Administration Set B. Braun Medical Inc. 242
Medex ICU Medical, Inc 237
Extension Set B. Braun Medical Inc. 171
MaxGuard BD Switzerland Sàrl 150
Medline Medline Industries, Inc. 148
Centurion Centurion Medical Products Corporation 145

Showing 12 of 768. All products under Set, Administration, Intravascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K000592 2001-04-12
K990388 1999-03-29
K982098 1999-03-01

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