Fluido® Compact

Fluido® Compact Standard Set with Drip Chamber

Registry build 21.09.26
1manufacturer
4catalogue numbers in this listing
2510(k) clearances naming this product code

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 Fluido® Compact
Listed by The Surgical Company International B.V., Netherlands
FDA product code LGZ
Device type Warmer, Thermal, Infusion Fluid
Device class Class 2
Regulation 21 CFR 880.5725
Establishment Specification developer, Manufacturer
Record published 2024-02-09
Record revised 2026-04-21 (version 2)

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, manufacturing date, serial number
Packaging Box of 30, box of 120, box of 15, box of 60

Catalogue Numbers

Catalogue numbers for Fluido® Compact
Catalogue number Size Status
Standard Set In distribution
Control Module In distribution
Warming Module In distribution
Standard Set with Drip Chamber 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
Astoflo® Plus ECO Stihler Electronic Gmbh 10
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

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
K252636 2025-11-18
K211618 2023-06-05

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