Primary Device ID | 07613327375404 |
NIH Device Record Key | 4ccfd60e-7bd3-4d47-9b71-fefea8f20c36 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AIR |
Version Model Number | 4720 |
Catalog Number | 4720 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327375404 [Primary] |
GAT | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2017-07-11 |
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