Navigator Aesthetic Delivery System

3 catalogue numbers from NAV-013, listed by Carticept Medical, Inc., United States, under Pump, Infusion. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
3catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Guangdong (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FRN
Manufacturer City Province Registered as Device types
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
JDI Electronics Factory Dongguan Guangdong Contract manufacturer 7
Zyno Electric & Machinery Ltd, Shanghai Shanghai Shanghai Contract manufacturer 1
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Record

Regulatory record for Navigator Aesthetic Delivery System
Listed by Carticept Medical, Inc., United States
FDA product code FRN
Device type Pump, Infusion
Device class Class 2
Regulation 21 CFR 880.5725
Record published 2017-02-24
Record revised 2023-10-18 (version 5)

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 Case of 25 of 25
Distribution end date 2017-11-04

Catalogue Numbers

Catalogue numbers for Navigator Aesthetic Delivery System
Catalogue number Size Status
NAV-013 Withdrawn
NAV-015 Withdrawn
NAV-038 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Port Access Infusion SET Sb-Kawasumi Laboratories, Inc. 76
Cadd ICU Medical, Inc 56
Flow Control Tubing GO Medical Industries PTY. Ltd. 39
Curlin Administration Set Zevex, Inc. 30
ambIT Summit Medical Products, Inc. 27
Beeline motIV Rex Pj Tech LLC 24
RMS Precision Flow Rate TubingTM Repro-Med Systems, Inc. 24
Medfusion ICU Medical, Inc 24
Volumat™ Line Fresenius Kabi AB 24
Outlook® B. Braun Medical Inc. 21
Alaris CareFusion 303, Inc 19
Alpha Source Battery Alpha Source Inc. 17

Showing 12 of 191. All products under Pump, Infusion

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K151255 2015-12-30
K124053 2013-03-13
K122215 2012-10-26
K120830 2012-04-16
K112067 2011-09-16
K101194 2011-07-11

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