Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

US

Last updated May 24, 2026

What WOONSOCKET PRESCRIPTION CENTER, INCORPORATED makes

The company manufactures unscented menstrual tampons and pads, antimicrobial and non-antimicrobial adhesive strips for skin coverage, adhesive bandages, non-woven gauze pads, and intermittent electronic patient thermometers. It also produces localized-body heating systems designed for electric pad use.

The portfolio includes devices classified as Class I, Class II, and unclassified (N/U), all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates within the United States, adhering to applicable regulatory requirements for these product categories.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Woonsocket Prescription Center, Incorporated manufacture?

Woonsocket Prescription Center, Incorporated produces a range of medical devices primarily focused on personal hygiene and minor wound care. Their portfolio includes unscented menstrual tampons and pads, adhesive bandages, non-woven gauze pads, and intermittent electronic patient thermometers. They also manufacture skin-cover adhesive strips (both antimicrobial and non-antimicrobial) and electric pad heating systems designed for localized-body heating. These devices are developed to address common health and comfort needs.

Where is Woonsocket Prescription Center, Incorporated based, and what regulatory requirements do they follow?

Woonsocket Prescription Center, Incorporated is based in the United States. As a manufacturer, they must comply with U.S. regulatory requirements applicable to their device categories, including those set by the FDA. Their products fall under classifications such as Class I, Class II, and unclassified (N/U), meaning they are subject to varying levels of oversight depending on their risk profile and intended use.

Are the devices manufactured by Woonsocket Prescription Center, Incorporated listed in any regulatory registries?

Yes, the devices produced by Woonsocket Prescription Center, Incorporated are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices classified as Class I, Class II, or unclassified (N/U), allowing healthcare providers, regulators, and patients to access standardized identification information for these products.

How are the devices from Woonsocket Prescription Center, Incorporated classified by the FDA?

The devices manufactured by Woonsocket Prescription Center, Incorporated are classified under three categories: Class I, Class II, and unclassified (N/U). Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls. Unclassified (N/U) devices are either not yet classified or fall outside standard FDA classification frameworks, meaning their regulatory pathway depends on their specific risk and purpose.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
952-890-1940
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
062312574

Catalogue (731)

Page 2 of 15
DeviceModel / ReferenceRegistriesClassStatus
CVS Health 893127
FDA UDI
Class IActive
CVS Health 717272
FDA UDI
Class IIActive
CVS Health 893120
FDA UDI
Class IActive
CVS Health Tampons BCVAP40
FDA UDI
Class IIActive
CVS Health Tampons BCVGR40
FDA UDI
Class IIActive
CVS Health CVS991271MYV1
FDA UDI
Class IActive
CVS Health Wide-Tip Triple Test Pregnancy Test Kit
FDA UDI
Class IIActive
CVS Health One Step Ovulation Test
FDA UDI
Class IActive
CVS Health 955443
FDA UDI
Class IUnknown
Cvs Health 715533-69755CV1
FDA UDI
Class IActive
CVS Health 540650
FDA UDI
Class IUnknown
CVS Health Triple Test Pregnancy Test Kit
FDA UDI
Class IIUnknown
CVS Health 964607
FDA UDI
Class IUnknown
CVS/Pharmacy KD-1760
FDA UDI
Class IIActive
CVS Liquid Bandage Spray 276670
FDA UDI
Class IActive
CVS Health 002024-511-002UC
FDA UDI
Class IIActive
CVS Health 1
FDA UDI
Class IActive
CVS Health Daily Ovulation Predictor
FDA UDI
Class IUnknown
CVSHealth BP3MW1-4BCVS
FDA UDI
Class IIActive
CVS Health 203385
FDA UDI
Class IIActive
Cvs Health 720078
FDA UDI
Class IActive
Cvs Health 842800
FDA UDI
Class IActive
CVS Health KI-8271.CVS
FDA UDI
Class IIActive
CVS Health 789270
FDA UDI
Class IUnknown
CVS Health Tampons BCVUR18
FDA UDI
Class IIActive
CVS Health 371287
FDA UDI
Class IUnknown
CVS Health MHP610S
FDA UDI
Class IIActive
CVS Health 844820
FDA UDI
Class IActive
CVS Health ULE
FDA UDI
Class IActive
CVS Health 199275
FDA UDI
Class IActive
CVS Health 731231
FDA UDI
Class IUnknown
CVS Health 235501
FDA UDI
Class IActive
CVS Health 955492
FDA UDI
Class IActive
CVS Health 262332
FDA UDI
Class IActive
CVS Health 551837
FDA UDI
UActive
CVS Health 375812
FDA UDI
Class IUnknown
Cvs Health Tampons CV12012UA
FDA UDI
Class IIActive
CVS Health 375807
FDA UDI
Class IActive
Revitalens 94233
FDA UDI
Class IIActive
CVS Health Six Days Sooner Pregnancy Test
FDA UDI
Class IIActive
CVS Health 459917
FDA UDI
Class IIActive
CVS Glucose Meter 8000-10753
FDA UDI
Class IIActive
CVS Health One Step Pregnancy Test
FDA UDI
Class IIUnknown
CVSHealth BP3KR1-4BCVS
FDA UDI
Class IIActive
Cvs Health 836893
FDA UDI
Class IActive
CVS Pharmacy Inc 995175
FDA UDI
Class IIActive
CVS Health NS18
FDA UDI
Class IIActive
CVS Health 935685
FDA UDI
Class IActive
CVS Health 893124
FDA UDI
Class IActive
CVS Health One Step Pregnancy Test
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.