Astoflo® Plus ECO

Blood and infusion warmer

Registry build 21.09.26
1manufacturer
10catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LGZ
Manufacturer City Province Registered as Device types
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24

Record

Regulatory record for Astoflo® Plus ECO
Listed by Stihler Electronic Gmbh, Germany
FDA product code LGZ
Device type Warmer, Thermal, Infusion Fluid
Device class Class 2
Regulation 21 CFR 880.5725
Establishment Complaint-file establishment, Manufacturer
510(k) K082765
Record published 2016-09-07
Record revised 2022-03-22 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Astoflo® Plus ECO
Catalogue number Size Status
AFP300UK In distribution
AFP300EU In distribution
WP31 In distribution
AFP302NA In distribution
WP33 In distribution
AFP302EU In distribution
AFP302UK In distribution
WP32 In distribution
WP34 In distribution
AFP300NA In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pedigo Products, Inc. Pedigo Products, Inc. 207
Amsco Steris Corporation 38
Level 1 ICU Medical, Inc 26
Skytron warming cabinet Skytron, LLC 24
ThermaCor 1200 Infusion System Smisson-Cartledge Biomedical LLC 11
enFlow Carefusion 8
Fluido® AirGuard System The Surgical Company International B.V. 7
Smithworks Medical, Inc. Smithworks, Inc. 5
Warming Cabinet Single Compartment Counter-Top Model (Glass Door) Imperial Surgical Ltd. 4
Hang&Go PAC Rand SPA 4
enFlow™ Airlife, Inc. 4
Enteral Feeding Medela LLC 4

Showing 12 of 159. All products under Warmer, Thermal, Infusion Fluid

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K082765 2008-12-18

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