Primary Device ID | 37613154881964 |
NIH Device Record Key | b3e3c5e4-f834-42e6-9c9e-d9337b9f7686 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0702045023 |
Catalog Number | 0702-045-023 |
Company DUNS | 196548481 |
Company Name | STRYKER CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613154881963 [Primary] |
GS1 | 37613154881964 [Package] Contains: 07613154881963 Package: pack [10 Units] In Commercial Distribution |
JCX | APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2016-09-23 |
07613327272246 - ARIA | 2025-09-25 IMPLANT IMPACTOR |
37613327405317 - SurgiCount Safety-Sponge | 2025-09-16 Laparotomy Sponge |
07613327262209 - XIA | 2025-09-11 FRENCH BENDER |
07613327262216 - XIA | 2025-09-11 SPREADER |
07613327262254 - XIA | 2025-09-11 COMPRESSOR |
07613327262261 - XIA | 2025-09-11 BLUNT PROBE |
07613327262292 - XIA | 2025-09-11 TORQUE WRENCH |
07613327262414 - XIA | 2025-09-11 STANDARD T-HANDLE |