Primary Device ID | 04546540756619 |
NIH Device Record Key | e986832e-42f7-4d9a-8914-1169dbd797e6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 234-030-049 |
Catalog Number | 234-030-049 |
Company DUNS | 187502109 |
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(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 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 1.5 Millimeter |
Length | 20 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540756619 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-09 |
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 |
07613327262438 - XIA | 2025-09-11 AWL |