Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006534724

FEI Number

3006534724

Entity Name

HANGZHOU YONINER PHARMACEUTICAL CO., LTD.

City/State/Country

HANGZHOU, ZHEJIANG, CN

Establishment Address

NANYANG ECONOMIC DEVEL. ZONE, XIAO SHAN, HANGZHOU, ZHEJIANG 311227, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

HANGZHOU YONINER PHARMACEUTICAL CO., LTD. (Owner Number: 9100042)

Owner / Operator Contact Address

NANYANG ECONOMIC DEVEL. ZONE, XIAO SHAN, HANGZHOU, CN-ZJ 311227, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ADHESIVE BANDAGE WOUND BANDAGE Nonwoven Roll Adhesive Dressing FIRST AID ADHESIVE TAPE FIRST AID KIT WITH DRUG FIRST AID KIT WITHOUT DRUG

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2007-04-06
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2013-12-16
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2024-05-20

Official Correspondent

JIN WEI

US Agent Details

CHARLES MACK Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

HANGZHOU YONINER PHARMACEUTICAL CO., LTD.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

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3012453673	FANNIN (UK) LIMITED	Measham, Swadlincote Derbyshire, GB
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006534724. Last updated year: 2026. Please use registration number 3006534724 when referencing this establishment in official correspondence.