Primary Device ID | 07613327512243 |
NIH Device Record Key | 70e2db18-2333-48ec-99bc-00015b3e513e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Connected OR HUB |
Version Model Number | 0240200101 |
Catalog Number | 0240200101 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
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 |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327512243 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-06-03 |
Device Publish Date | 2021-05-26 |
07613327419153 | 0240200103 |
07613327419146 | 0240200102 |
07613327512243 | 0240200101 |
07613327413281 | Device Management Control System |