Primary Device ID | 07613327455915 |
NIH Device Record Key | 76476022-c0de-476a-90ee-36d6532b9e7a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | L11 |
Version Model Number | 0220230300 |
Catalog Number | 0220230300 |
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 | false |
Serial Number | true |
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 | 07613327455915 [Primary] |
OWN | Confocal optical imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2019-01-21 |
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