
E-Z-Em, Inc.
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FLEXI-THERM FILM is an FDA 510(k)-cleared medical device (K770986) manufactured by E-Z-Em, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 11, 1977. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
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Hollister
SKU VM-1270031