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REDI-FLEX
 Request for Information Form |
 Contact Information
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| Company Name | REDI-TECH MEDICAL PRODUCTS, LLC |
| Address | 529 FRONT ST.
SUITE 125 |
| City, State, Zip | CLEVELAND, OH 44017 |
| Country | US |
| FDA Owner/Operator Phone | 800-824-1793 |
| FDA Medical Specialty Code | GU - Gastroenterology/Urology |
| FDA Product Code | FKO |
| FDA Classification Name | CATHETER, PERITONEAL DIALYSIS, SINGLE USE |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 876.5630 |
| FDA Common Generic Name | PERITONIAL DIALYSIS CATHETER OR P-D CATHETER |
| FDA Proprietary Device Name | REDI-FLEX |
| FDA Owner / Operator Number | 9072276 |
| FDA Owner / Operator Name | REDI-TECH MEDICAL PRODUCTS, LLC |
| FDA Establishment Registration Number | 3005137477 |
| FDA Registered Establishment Name | REDI-TECH MEDICAL PRODUCTS, LLC |
| FDA Operation Code(s) |
RR - Repackager/Relabeller |
| FDA Listing Date | 06-06-05 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of REDI-TECH MEDICAL PRODUCTS, LLC
Our records indicate that the following medical device companies may manufacture a similar device.
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