Question 1

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

Accepted Answer

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.

Question 2

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

Accepted Answer

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.

Question 3

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

Accepted Answer

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.

Question 4

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

Accepted Answer

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.

Device	Model / Reference	Registries	Class	Status
CVS Health	445417	FDA UDI	U	Unknown
CVS Health	733523/16CVS01421	FDA UDI	Class I	Active
CVS Health	UVH	FDA UDI	Class I	Unknown
CVS Health	275172	FDA UDI	Class II	Active
CVS Health	159520	FDA UDI	N	Active
CVS Health	951345	FDA UDI	Class I	Unknown
CVS Health	800231	FDA UDI	Class II	Active
Cvs Health	246000	FDA UDI	Class I	Active
CVS Health	444830	FDA UDI	Class I	Unknown
CVS Health	702514	FDA UDI	Class I	Active
CVS Health	241628	FDA UDI	Class I	Active
CVS Health	216515	FDA UDI	Class I	Active
CVS Health	364089	FDA UDI	N	Unknown
CVS/Pharmacy	KD-1342	FDA UDI	Class II	Active
CVS Pharmacy	920126	FDA UDI	Class I	Active
CVS Health	Advanced One Step Pregnancy Test	FDA UDI	Class II	Active
CVS Health	209391	FDA UDI	Class I	Active
Cvs	344596	FDA UDI	N	Active
CVS Health	BCVAS54	FDA UDI	Class II	Unknown
CVSHealth	616274	FDA UDI	Class I	Active
CVS Health	366398	FDA UDI	Class I	Active
Cvs Health Tampons	CV12012SA	FDA UDI	Class II	Active
Cvs Health	427504_70274CV	FDA UDI	N/A	Active
CVS Health	RMH	FDA UDI	Class I	Active
CVS Health	762146	FDA UDI	Class I	Active
CVS Health	375812	FDA UDI	Class I	Active
CVS Friction Guard Spray	471164	FDA UDI	Class I	Active
CVS Health	830963	FDA UDI	Class I	Active
CVS Health	383505	FDA UDI	Class I	Active
CVS Health	951341	FDA UDI	U	Active
CVS Pharmacy Inc	378525	FDA UDI	Class II	Active

WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

What WOONSOCKET PRESCRIPTION CENTER, INCORPORATED makes

Frequently asked questions

Information

Catalogue (731)

Related Companies

Authorised Representatives

Importers

Notified Bodies

Authorities