Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9610649

FEI Number

3002807578

Entity Name

MEDICAL WIRE AND EQUIPMENT CO. LTD.

City/State/Country

CORSHAM, WILTSHIRE, GB

Establishment Address

POTLEY, CORSHAM, WILTSHIRE SN13 9RT, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MEDICAL WIRE AND EQUIPMENT CO. LTD. (Owner Number: 8021919)

Owner / Operator Contact Address

POTLEY, --, CORSHAM, WILTSHIRE, GB-NOTA SN13 9RT, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Culture Medium Culture Medium Applicator Transwab Viabank Isolation Supplements Microring (Except for YT) Polycon; Fecon; Boricon Dry Swab Micro Loops Collector Applicator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JSJ	Culture Media, Selective And Non-Differential	Microbiology	Class 1	866.2360	1992-11-13
JSI	Culture Media, Selective And Differential	Microbiology	Class 1	866.2360	1992-11-13
KCJ	Applicator, Ent	Ear, Nose, Throat	Class 1	874.5220	1992-11-13
JSL	Culture Media, Anaerobic Transport	Microbiology	Class 1	866.2390	2007-12-10
JTR	Kit, Quality Control For Culture Media	Microbiology	Class 1	866.2480	2002-07-25
JSK	Supplement, Culture Media	Microbiology	Class 1	866.2450	2002-07-25
LIB	Device, General Purpose, Microbiology, Diagnostic	Microbiology	Class 1	866.2660	2002-07-25
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2002-07-25
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2006-11-17
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2002-07-25
LIO	Device, Specimen Collection	Microbiology	Class 1	866.2900	2009-01-30
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	1992-11-13

Official Correspondent

No official correspondent registered.

US Agent Details

Carol Buchert Business: MDC Associates, Inc. Email: Reglist@mdcassoc.com Phone: (978) 9273808

Related Public Records

Same Entity

MEDICAL WIRE AND EQUIPMENT 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
K863524	Bd Becton Dickinson Vacutainer Systems Preanalytic	REGAN-LOWE CHARCOAL AGAR	1986-09-19
K862389	Otisville Biotech, Inc.	BIOTIS ACETAMIDE AGAR	1986-07-03
K811644	Hardy Media	HEKTOEN ENTERIC AGAR	1981-07-02
K832535	Otisville Biotech, Inc.	HEKTOEN ENTERIC AGAR PLATE	1983-10-04
K811331	Acumedia Manufacturers, Inc.	SF BROTH	1981-05-29

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

Similar Registrations

Registration Number	Establishment Name	Location
3005182159	HIMEDIA LABORATORIES PRIVATE LIMITED	NASHIK Maharashtra, IN
1924669	REMEL, INC.	LENEXA, KS, US
1210083	ANALYTICHEM USA, INC.	Winslow, ME, US
8010096	OXOID, LTD.	BASINGSTOKE, HAMPSHIRE, GB
3017871324	HIMEDIA LABORATORIES PRIVATE LIMITED	Thane Maharashtra, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9610649. Last updated year: 2026. Please use registration number 9610649 when referencing this establishment in official correspondence.