SHANGHAI LONGMANN TECH CO., LTD.

FDA Device Registration & Listing · Shanghai, CN · Registration 3018226067

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
3018226067
FEI Number
3018226067
Entity Name
SHANGHAI LONGMANN TECH CO., LTD.
City/State/Country
Shanghai, CN
Establishment Address
Room 2106, No. 3, Lane 791, Lingling Road, Shanghai 200030, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
SHANGHAI LONGMANN TECH CO., LTD. (Owner Number: 10094176)
Owner / Operator Contact Address
Room 2106, No. 3, Lane 791, Lingling Road, Shanghai, CN-SH 200030, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CuffTrek LG-I

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BSK Cuff, Tracheal Tube, Inflatable Anesthesiology Class 2 868.5750 2025-11-17

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

SHANGHAI LONGMANN TECH CO., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2014 H & H Associates 2
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part ***H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708***. The product is used to maintain fracture alignment.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018226067. Last updated year: 2026. Please use registration number 3018226067 when referencing this establishment in official correspondence.
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