TONGXIANG DAFUGUI MEDICAL SUPPLIES FACTORY

FDA Device Registration & Listing · Jiaxing City Zhejiang, CN · Registration 3045076483

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
3045076483
FEI Number
3045076483
Entity Name
TONGXIANG DAFUGUI MEDICAL SUPPLIES FACTORY
City/State/Country
Jiaxing City Zhejiang, CN
Establishment Address
50m East, No.5 Bridge, Chonggao Road, Chongfu Town, Tongxiang City, Jiaxing City Zhejiang 314511, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TONGXIANG DAFUGUI MEDICAL SUPPLIES FACTORY (Owner Number: 10095779)
Owner / Operator Contact Address
50m East, No.5 Bridge, Chonggao Road, Chongfu Town, Tongxiang City, Jiaxing City, CN-ZJ 314511, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dressing, Wound dressing, Medical dressing, Adhesive dressing, Sterile dressing, Non-adherent dressing, Island dressing Skin closure strip, Wound closure strip, Suture strip, Adhesive skin closure, Butterfly stitch, butterfly bandage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2026-04-28
QQS Stapler, Skin General Hospital Class 1 878.4740 2026-04-28

Official Correspondent

Stella Stella

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

TONGXIANG DAFUGUI MEDICAL SUPPLIES FACTORY
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
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019 COVIDIEN LLC 1
Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0017-2019 COVIDIEN LLC 1
Dermacea Gauze Fluff Roll, 6 Ply, 4-1/2 x 4-1/8 yd (11.4 cm x 3.7 m), REF 441103 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3045076483. Last updated year: 2026. Please use registration number 3045076483 when referencing this establishment in official correspondence.
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