Primary Device ID | 00817369021795 |
NIH Device Record Key | ed789d0a-0e44-4586-9dd3-c8e6b228790f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NormaTec MVP Pro Upper and Lower Body Recovery Package |
Version Model Number | MVP Pro Recovery Package - Upper and Lower Body Po |
Catalog Number | 40433 |
Company DUNS | 111448069 |
Company Name | NORMATEC INDUSTRIES LP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817369021795 [Primary] |
JOW | Sleeve, Limb, Compressible |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-14 |
00817369021818 | MVP Pro Recovery Package - Upper and Lower Body Power Tall |
00817369021801 | MVP Pro Recovery Package - Upper and Lower Body Power Standard |
00817369021795 | MVP Pro Recovery Package - Upper and Lower Body Power Short |
00817369021788 | MVP Pro Recovery Package - Upper and Lower Body Short |
00817369021771 | MVP Pro Recovery Package - Upper and Lower Body Tall |
00817369021764 | MVP Pro Recovery Package - Upper and Lower Body Standard |