Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009750077

FEI Number

3009750077

Entity Name

NANJING TIANAO MEDICAL INSTRUMENTS MANUFACTURE CO.,LTD

City/State/Country

Nanjing Jiangsu, CN

Establishment Address

Changqiao Rd.,Qiaolin Industry Park, Pukou District, Nanjing Jiangsu 211806, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

NANJING TIANAO MEDICAL INSTRUMENTS MANUFACTURE CO.,LTD (Owner Number: 10041181)

Owner / Operator Contact Address

Changqiao Rd.,Qiaolin Industry Park, Pukou District, Nanjing, CN-JS 211806, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

proCARE Central E-Lock Frame proCARE Basic Frame proCARE Emergency Code Response Cart proCARE Manual Lock Frame proCARE Pediatric Code Response Cart proCARE Anesthesia Cart proCARE Isolation Cart proCARE Intelligent Anesthesia Cart proCARE General Procedure Cart proCARE Single Level Lock Frame proCARE General Procedure Cart, E-Lock proCARE Intelligent Procedure Cart proCARE Single Level Lock Frame with PC proCARE Emergency Frame proCARE Central E-Lock Frame with PC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BZN	Cart, Emergency, Cardiopulmonary (Excluding Equipment)	Anesthesiology	Class 1	868.6175	2021-11-02

Official Correspondent

Guangjun Zhang

US Agent Details

Jordan Smith Business: Touchpoint Medical Inc dba iTD USA Email: jsmith@touchpointmed.com Phone: (813) 5601146

Related Public Records

Same Entity

NANJING TIANAO MEDICAL INSTRUMENTS MANUFACTURE CO.,LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009750077. Last updated year: 2026. Please use registration number 3009750077 when referencing this establishment in official correspondence.