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Sign in to claim this brandMerrithew International Inc
Canada·CA-MF-000005225
Last updated September 18, 2026
About
Merrithew's Pilates equipment is globally renowned by clients in fitness, health care & hospitality. Shop online for Reformers, chairs, accessories & more
From the manufacturer's own website. Source
What Merrithew International Inc makes
Merrithew International Inc manufactures Pilates reformers and related equipment bundles, including models such as the Rehab V2 Max, V2 Max Plus, SPX Max, and Core One-on-One Studio systems. These products are designed for use in fitness, rehabilitation, and studio settings, with configurations varying by frame, ropes, and included accessories.
The manufacturer's devices are classified as Class I medical devices and are listed in the EUDAMED registry. The company is based in Canada.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of products does Merrithew International Inc manufacture?
Merrithew International Inc produces Pilates reformers and related equipment bundles, such as the Rehab V2 Max, V2 Max Plus, SPX Max, and Core One‑on‑One Studio systems. The answer is based on the device list, which shows only reformer‑type frames, bundles, and accessories, indicating the company’s focus on Pilates equipment.
Where is Merrithew International Inc headquartered?
The company is based in Canada, as indicated by the COUNTRY field in the provided data. This location is explicitly stated and therefore is the only reliable source for the company's headquarters.
In which regulatory registry are Merrithew’s devices listed?
Merrithew’s devices appear in the EUDAMED registry. The data lists "LISTED IN: eudamed," which means the company's Class I medical devices are recorded in the European Union’s database for medical devices.
How are Merrithew’s Pilates devices classified under medical device regulations?
All of Merrithew’s listed products are classified as Class I medical devices. This classification is directly taken from the DEVICE CLASSES entry, indicating they are considered low‑risk devices under the applicable regulatory framework.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Canada
- Address
- 1271, Tapscott Rd, Scarborough, Canada
- Website
- HTTPS://WWW.MERRITHEW.COM
- linkedin.com/company/merrithew
- facebook.com/merrithew
- [email protected]
- Phone
- +14164824050
- PRRC Contact
- RANDY AULD
- EUDAMED SRN
- CA-MF-000005225
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (57)
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