Primary Device ID | 00889024406636 |
NIH Device Record Key | f3b54dd7-c11d-415f-bbc4-60208e55cd33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCP |
Version Model Number | 614.582 |
Company DUNS | 078836317 |
Company Name | ZIMMER KNEE CREATIONS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Handling Environment Temperature | Between 59 Degrees Fahrenheit and 77 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024205390 [Primary] |
GS1 | 00889024406636 [Package] Contains: 00889024205390 Package: [4 Units] In Commercial Distribution |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-23 |
00889024406650 | 614.584 |
00889024406667 | 614.541 |
00889024406643 | 614.583 |
00889024406636 | 614.582 |
00889024406629 | 614.581 |
00889024406612 | 514.303 |
00889024406605 | 514.302 |
00889024205284 | 402.201 |