Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016712364

FEI Number

3016712364

Entity Name

HAGUE GLOBAL LIMITED

City/State/Country

Ipswich Suffolk, GB

Establishment Address

C/O 6th Floor St Vincent House, 1 Cutler Street, Ipswich Suffolk IP1 1UQ, GB

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Hague Global Limited (Owner Number: 10087001)

Owner / Operator Contact Address

C/O 6th Floor St Vincent House, 1 Cutler Street, Ipswich, GB-SFK IP1 1UQ, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

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Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JJB	Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.)	Clinical Chemistry	Class 1	862.1115	2024-11-08
INO	Chair, Positioning, Electric	Physical Medicine	Class 2	890.3110	2024-08-07
JRE	Refractometer For Clinical Use	Clinical Chemistry	Class 1	862.2800	2024-11-08
JMT	Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)	Clinical Chemistry	Class 1	862.1510	2024-11-08
LJX	Test, Urine Leukocyte	Hematology	Class 1	864.7675	2024-11-08
JIR	Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)	Clinical Chemistry	Class 1	862.1645	2024-11-06
JIN	Nitroprusside, Ketones (Urinary, Non-Quant.)	Clinical Chemistry	Class 1	862.1435	2024-11-08
KME	Bedding, Disposable, Medical	General Hospital	Class 1	880.6060	2023-05-04
JMA	Acid, Ascorbic, 2,4-Dinitrophenylhydrazine (Spectrophotometric)	Clinical Chemistry	Class 1	862.1095	2024-11-08
CEN	Dye-Indicator, Ph (Urinary, Non-Quantitative)	Clinical Chemistry	Class 1	862.1550	2024-11-08

Official Correspondent

Angus Hague

US Agent Details

Joyce Kwon Business: Provision Consulting Group, Inc. Email: ask@provisionfda.com Phone: (909) 4933276

Related Public Records

Same Entity

Hague Global Limited

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
K885053	Biotrol, USA, Inc.	BIOTROL URINE PROTEINS REAGENT	1989-01-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016712364. Last updated year: 2026. Please use registration number 3016712364 when referencing this establishment in official correspondence.