Moss

Moss MarkIV Nasal Tube

Registry build 21.09.26
1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Zhejiang.

Chinese manufacturers registered for FDA product code BSS
Manufacturer City Province Registered as Device types
Ningbo Tianyi Medical Appliance Co., Ltd. Ningbo Zhejiang Contract manufacturer 11

Record

Regulatory record for Moss
Listed by Moss Tubes, Inc., United States
FDA product code BSS
Device type Tube, Nasogastric
Device class Class 2
Regulation 21 CFR 876.5980
Establishment Specification developer, Manufacturer
510(k) K984629
Record published 2017-10-04
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Sizes Catheter gauge 18 Fr

Catalogue Numbers

Catalogue numbers for Moss
Catalogue number Size Status
6-87168 Catheter Gauge 18 Fr In distribution

Same Product Code

Showing 12 of 20. All products under Tube, Nasogastric

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K984629 1999-03-02

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