Primary Device ID | 37613327465854 |
NIH Device Record Key | ad74df92-a4ee-4484-ba8e-700b0ea323c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SurgiCount Safety-Sponge |
Version Model Number | 0611008108 |
Catalog Number | 0611-008-108 |
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 |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM | |
Phone | +0118002533210 |
INST.STRYKER.CS@STRYKER.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327465853 [Primary] |
GS1 | 37613327465854 [Package] Contains: 07613327465853 Package: case [40 Units] In Commercial Distribution |
GDY | Gauze/sponge, internal, x-ray detectable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-09-11 |
Device Publish Date | 2025-09-03 |