Primary Device ID | 07613327261592 |
NIH Device Record Key | 5a8f5b9a-1ebb-4b15-be3a-bcd3e29d9915 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 6254 |
Catalog Number | 6254-000-000 |
Company DUNS | 078470558 |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327261592 [Primary] |
FPP | STRETCHER, HAND-CARRIED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
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