Primary Device ID | 37613327374446 |
NIH Device Record Key | 97c97396-600b-469f-8a7d-51529eff5768 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0306813000 |
Catalog Number | 0306813000 |
Company DUNS | 196548481 |
Company Name | STRYKER CORPORATION |
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 | 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 |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Needle Gauge | 13 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327374445 [Primary] |
GS1 | 37613327374446 [Package] Contains: 07613327374445 Package: pack [6 Units] In Commercial Distribution |
OCJ | spinal channeling instrument, vertebroplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-05-07 |
Device Publish Date | 2018-04-04 |
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