SpiroScout SP Plus

The SpiroScout SP plus is intended exclusively for use with the following SCHILLER devices. CARDIOVIT CS-104 SPIROVIT SP-1 G2 CARDIOVIT AT-102 G2 The SpiroScout SP plus is an ultrasonic…

Registry build 21.09.26

The SpiroScout SP plus is intended exclusively for use with the following SCHILLER devices. CARDIOVIT CS-104 SPIROVIT SP-1 G2 CARDIOVIT AT-102 G2 The SpiroScout SP plus is an ultrasonic measuring system which is used for pulmonary function diagnostics. It determines the transit times of the ultrasonic signals and can be used with the above-mentioned Schiller devices to measure and analyse respiratory flow and volume.

10manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (5), Guangdong (3), Fujian (1). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BZG
Manufacturer City Province Registered as Device types
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Intersurgical Medical Apparatus (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 12
Ningbo Tianyi Medical Appliance Co., Ltd. Ningbo Zhejiang Contract manufacturer 11
GVS Technology (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Flexible Circuit Technologies Shenzhen Shenzhen Guangdong Contract manufacturer 1
Changshu Rozer Sterilization Technology Co., Ltd. Changshu Jiangsu Contract manufacturer 43
Rozer Sterilization Technology Shuyang Company Limited Shuyang Jiangsu Contract manufacturer 33
Feellife Health Inc. Shenzhen Guangdong Contract manufacturer 8

Record

Regulatory record for SpiroScout SP plus
Listed by Ganshorn Medizin Electronic Gmbh, Germany
FDA product code BZG
Device type Spirometer, Diagnostic
Device class Class 2
Regulation 21 CFR 868.1840
Establishment Manufacturer
510(k) K160116
Record published 2021-12-20
Record revised 2022-03-08 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Storage environment humidity 10 to 95 % RH; Storage environment temperature -20 to 50 °C; Storage environment atmospheric pressure 60 to 105 KiloPascal

Catalogue Numbers

Catalogue numbers for SpiroScout SP plus
Catalogue number Size Status
Rev.D In distribution
D In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Polytech Filter Polytechnic Resources, Inc. 190
Model 4000 Vitalograph Ireland Ltd. 115
Astra Spirometer S D I Diagnostics Inc 90
MIR Mir Medical International Research 56
Curaplex TRI-Anim Health Services, Inc. 55
Alpha Vitalograph Ireland Ltd. 48
Welch Allyn, Inc. Welch Allyn, Inc. 47
MGC Diagnostics Medical Graphics Corp. 42
Astraguard S D I Diagnostics Inc 39
PFT Vitalograph Ireland Ltd. 38
Vyaire Jaeger Medical GmbH 36
BVF Vitalograph Ireland Ltd. 29

Showing 12 of 123. All products under Spirometer, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160116 2016-10-07

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