HANGHAI MEDICAL PRODUCTS CO LTD

FDA Device Registration & Listing · Jinhua City Zhejiang, CN · Registration 3009563903

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009563903
FEI Number
3009563903
Entity Name
HANGHAI MEDICAL PRODUCTS CO LTD
City/State/Country
Jinhua City Zhejiang, CN
Establishment Address
Bailongqiao Industry Park, Jinhua City Zhejiang 321025, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hanghai Medical Products Co Ltd (Owner Number: 10040401)
Owner / Operator Contact Address
Bailongqiao Industry Park, Jinhua City, CN-ZJ 321025, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Surgical Tape; Cohesive Bandages; Sport Tape KN95 Protective Mask Face Mask Cooling Patch Wound Dressing Face Mask For General Public/Healthcare Personnel

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 2012-05-15
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2020-03-27
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-03-10
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2012-11-16
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2012-04-09
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-04-08

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Hanghai Medical Products 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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009563903. Last updated year: 2026. Please use registration number 3009563903 when referencing this establishment in official correspondence.
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