About Phase II
The Company
Founded in 1995 to serve the single-use medical product and device industry, Phase II
Medical Manufacturing now provides design, development, manufacturing, packaging,
shipping, and sterilization services to its customers. FDA registration, Canadian
licensing, and ISO 9001:2000 and ISO 13485:2003 certification are maintained to ensure
that current U.S. and international standards are satisfied.
Phase II works directly with clients on a regular basis to ensure all devices meet the appropriate specifications, and our commitment and dedication to our customers has proven to be highly successful. Since its inception Phase II has grown tenfold and, in 2004, moved from our original location in a Rollinsford, New Hampshire mill building to a newer Rochester, NH facility with double the space.
- ISO Certificate ISO9001
- ISO Certificate ISO13485-2003
- FDA Registration Search (search for Registration Number 1225492)
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Notified Body Information |
Authorized European Representative Information |
