Primary Device ID | 37613327570480 |
NIH Device Record Key | c35553e8-ac5a-48a4-a717-cfb22a98cf4b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pivot Guardian |
Version Model Number | 3105000741 |
Catalog Number | 3105-000-741 |
Company DUNS | 187502109 |
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 | 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 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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Phone | +1(866)624-4422 |
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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 | |
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 | 07613327570489 [Primary] |
GS1 | 37613327570480 [Package] Contains: 07613327570489 Package: pack [3 Units] In Commercial Distribution |
HST | Apparatus, traction, non-powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-09 |
Device Publish Date | 2022-06-01 |
07613327419689 | 3105000201 |
37613327419048 | Pivot Guardian Disposable Kit, Medium |
37613327419031 | Pivot Guardian Disposable Kit, Large |
37613327419024 | Pivot Guardian Disposable Kit, Small |
07613327380385 | PostFree Tabletop Extension, US |
07613327380378 | PostFree Perineal Accessory Kit |
07613327380361 | PostFree Frame |
37613327376402 | PostFree Patient Safety Kit, Large |
37613327376396 | PostFree Patient Safety Kit, Medium |
37613327376389 | PostFree Patient Safety Kit, Small |
07613327575484 | 3105000303 |
07613327574838 | 3105000304 |
07613327565812 | 3105000300 |
07613327565782 | 3105000313 |
07613327565775 | 3105000301 |
07613327565379 | 3105000306 |
07613327563818 | 3105000308 |
37613327570480 | Pivot Guardian Direct Disposable Kit Medium |
37613327570473 | Pivot Guardian Direct Disposable Kit Large |
37613327570466 | Pivot Guardian Direct Disposable Kit Small |
07613327581539 | 3105000305 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PIVOT GUARDIAN 90712541 not registered Live/Pending |
Stryker Corporation 2021-05-14 |