Medisystems Hemodialysis Fistula Needle Set

3 catalogue numbers from S9-5005, listed by Medisystems Corp., United States, under Needle, Fistula. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
3catalogue numbers in this listing
6510(k) clearances naming this product code
1recall

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code FIE
Manufacturer City Province Registered as Device types
Guangzhou Huada Biotechnology Co., Ltd. Guangzhou Guangdong Contract manufacturer 9
Guangzhou Kaiheng K&S Co., Ltd. Guangzhou Guangdong Contract manufacturer 9
Bain Medical Equipment(Guangzhou) Co., Ltd. Guangzhou Guangdong Manufacturer 3
Vital Healthcare (Guangzhou) Co., Ltd. Guangzhou Guangdong Contract manufacturer 3

Record

Regulatory record for Medisystems Hemodialysis Fistula Needle Set
Listed by Medisystems Corp., United States
FDA product code FIE
Device type Needle, Fistula
Device class Class 2
Regulation 21 CFR 876.5540
Record published 2016-09-16
Record revised 2021-02-19 (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
Storage Special storage condition: Keep dry; Storage environment temperature 0 to 40 °C
Packaging Pack of 250
Sizes Length 1 in; needle gauge 15 to 17 G
Distribution end date 2020-12-31

Catalogue Numbers

Catalogue numbers for Medisystems Hemodialysis Fistula Needle Set
Catalogue number Size Status
S9-5005 Length 1 in Withdrawn
S9-5007 Length 1 in Withdrawn
S9-5006 Length 1 in Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medisystems Hemodialysis Fistula Needle Set with MasterGuard Medisystems Corp. 72
Medisystems TwinPack Hemodialysis Fistula Needle Set with MasterGuard Medisystems Corp. 44
masterguard plus Hemodialysis Fistula Needle SET Nxstage Medical, Inc. 35
masterguard plus Twinpack+ Hemodialysis Fistula Needle Sets Nxstage Medical, Inc. 20
Dora Bain Medical Equipment(Guangzhou) Co., Ltd. 17
JMS Wingeater A.v.fistula Needle SET JMS Singapore PTE. Ltd 15
Medisystems Button Hole Needle Set Medisystems Corp. 14
ButtonHole with SteriPick Twinpack+ Needle SET Nxstage Medical, Inc. 14
Medisystems TwinPack ButtonHole Needle Set with SteriPick Medisystems Corp. 14
ButtonHole with SteriPick Needle SET Nxstage Medical, Inc. 14
Medisystems Button Hole Needle Set with SteriPick Medisystems Corp. 14
JMS A.V. Fistula Needle SET JMS Singapore PTE. Ltd 11

Showing 12 of 32. All products under Needle, Fistula

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K062953 2007-02-12
K990803 2000-01-06
K932074 1994-02-18
K910734 1991-06-20
K862002 1986-06-27
K811838 1981-09-08

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
2012-01-31 Not classified Employee error Mislabeled outer carton: Outside shipping cartons is stamped 15Ga x 1″, product contained within properly labeled as 17Ga x 1″ needle 20,750 units (83 cases) 2012-09-12

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