Pharmapac (UK) Ltd

FDA Device Registration & Listing · Bidston Wirral, GB · Registration 3004610510

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
3004610510
FEI Number
3004610510
Entity Name
Pharmapac (UK) Ltd
City/State/Country
Bidston Wirral, GB
Establishment Address
Unit 22, Valley Road Business Park, Bidston Wirral CH41 7EL, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Pharmapac (UK) Ltd (Owner Number: 10032965)
Owner / Operator Contact Address
Unit 22, Valley Road Business Park, Bidston, GB-WRL CH41 7EL, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stomahesive Powder

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EXE Protector, Ostomy Gastroenterology, Urology Class 1 876.5900 2010-06-29

Official Correspondent

No official correspondent registered.

US Agent Details

James Martin Biggs Business: GBM Authorized Representative Ltd. Email: caroline@mba-gbm.com Phone: (405) 7771033

Related Public Records

Same Entity

Pharmapac (UK) Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004610510. Last updated year: 2026. Please use registration number 3004610510 when referencing this establishment in official correspondence.
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