Primary Device ID | 00889024504653 |
NIH Device Record Key | f3d36811-e0b4-48f9-97ed-606cf792fce3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ActiveCare® DVT |
Version Model Number | A502B000111 |
Catalog Number | A502B000111 |
Company DUNS | 137354267 |
Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. |
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 | false |
Manufacturing Date | false |
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 | 00889024504653 [Primary] |
JOW | SLEEVE, LIMB, COMPRESSIBLE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-04 |
Device Publish Date | 2019-02-01 |
00889024504653 | A502B000111 |
00889024504646 | A502B000109 |
00889024504622 | A502B000105 |
00889024504615 | A502B000103 |
00889024504530 | A502B000102 |