PF 5001 Main Unit

Catalogue number PF 5001, listed by Perimed AB, Sweden, under Flowmeter, Blood, Cardiovascular. 4 manufacturers in China are registered for this product code.

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

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code DPW
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Helen of Troy Macao Limited Macau Guangdong Private-label distributor 11
Dongguan Mars Medical Products Co., Ltd. Dongguan Guangdong Manufacturer 9
Onbo Electronic (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 6

Record

Regulatory record for PF 5001 Main Unit
Listed by Perimed AB, Sweden
FDA product code DPW
Device type Flowmeter, Blood, Cardiovascular
Device class Class 2
Regulation 21 CFR 870.2100
Establishment Complaint-file establishment, Manufacturer
510(k) K974285
Record published 2016-09-13
Record revised 2026-03-17 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date, serial number
Storage Storage environment temperature 0 to 50 °C; Storage environment humidity 30 to 85 % RH
Distribution end date 2023-02-01

Catalogue Numbers

Catalogue numbers for PF 5001 Main Unit
Catalogue number Size Status
PF 5001 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Transonic Transonic Systems, Inc. 627
SonoTT Vascular Probe Em-Tec GmbH 12
BiDop 7 probe Koven Technology, Inc. 8
Medistim MiraQ Cardiac System Medistim ASA 6
Medistim MiraQ Vascular System Medistim ASA 6
FlowMet™ Medtronic, Inc. 4
GEM Flow Coupler Synovis Micro Companies Alliance 4
CooperSurgical® Coopersurgical, Inc. 4
Medistim System Activation Card Medistim ASA 3
811-BL 24V Foreign & Domestic Parks Medical Electronics, Inc. 3
Medistim MiraQ Ultimate System Medistim ASA 3
Dopplex Huntleigh Healthcare Ltd. 3

Showing 12 of 154. All products under Flowmeter, Blood, Cardiovascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152930 2016-05-05
K011899 2001-11-06
K974285 1998-05-28
K932068 1993-12-07
K922368 1993-02-03
K890828 1989-06-20

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