PICO50

PICO50 Arterial blood sampler, 2 mL, box of 100 units

Registry build 21.09.26
23manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (7), Zhejiang (6), Shanghai (3). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JKA
Manufacturer City Province Registered as Device types
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3
Tianjin Hanaco Medical Co., Ltd. Tianjin Tianjin Contract manufacturer 3
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Medicines & Health Products I/ E Co., Ltd. Hangzhou Zhejiang Exporter 41
Jiangsu Caina Medical Co., Ltd. Jiangyin Jiangsu Contract manufacturer 20
Hangzhou Best Valley Medical Technology Co., Ltd. Hangzhou Zhejiang Exporter 20
Zhejiang Kindly Medical Devices Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Jiangsu Rongye Technology Co., Ltd. Yangzhou Jiangsu Manufacturer 16
Yangzhou Medline Industry Co., Ltd. Yangzhou Jiangsu Contract manufacturer 11
Shanghai Mekon Medical Devices Co., Ltd. Shanghai Shanghai Exporter 11

Showing 12 of 23. All 23 manufacturers in China registered for Tubes, Vials, Systems, Serum Separators, Blood Collection

Record

Regulatory record for PICO50
Listed by Radiometer Medical APS, Denmark
FDA product code JKA
Device type Tubes, Vials, Systems, Serum Separators, Blood Collection
Device class Class 2
Regulation 21 CFR 862.1675
Establishment Complaint-file establishment, Manufacturer
Record published 2016-09-01
Record revised 2022-11-01 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 32 °C
Distribution end date 2022-10-11

Catalogue Numbers

Catalogue numbers for PICO50
Catalogue number Size Per pack Status
956-552 100 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Portex ICU Medical, Inc 182
S-Monovette® Sarstedt Aktiengesellschaft & Co.KG 108
Vacuette Greiner BIO-ONE Gmbh 106
Jelco ICU Medical, Inc 35
Kbmed KB Medical (Group) Inc. 33
Marketlab Inc Marketlab Incorporated 30
Maveric Medical Maveric Medical LLC 27
Safe-T-Fill® Ram Scientific 23
Improvacuter® Gel & Clot Activator Tube Guangzhou Improve Medical Instruments Co., Ltd. 21
Medline Medline Industries, Inc. 20
Kurin Blood Culture Collection Set Kurin, Inc. 20
Reli Myco Medical Supplies, Inc. 18

Showing 12 of 303. All products under Tubes, Vials, Systems, Serum Separators, Blood Collection

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K043143 2005-04-22

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of PICO50
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Radiometer Medical APS UDI-DI 2022-04-08 Class II Package design/selection Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product. 7,228 boxes (100 units per box)

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. 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
2021-03-26 Class II Under Investigation by firm Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler. The issue relates to the sterile barrier system for the product. During internal stress testing on PICO70 Arterial Blood Samplers a breach in the sterile barrier sy 348,178 boxes worldwide (1,883 boxes in the U.S.) 2023-03-01

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