| Primary Device ID | 07613327056921 |
| NIH Device Record Key | 1aeb170d-b98f-42db-ac5c-152c9fb8f640 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SERFAS Energy |
| Version Model Number | 0279350401 |
| Catalog Number | 279-350-401 |
| 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 | |
| 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 |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Length | 135 Millimeter |
| Outer Diameter | 3.5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327056921 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
| 07613327405828 | 50-S Sweep + XL, Suction Probe, Non-Bendable, XL/Hip Length |
| 07613327405811 | 50-S Sweep +, Suction Probe, Non-Bendable. |
| 07613327060904 | Probe Bender |
| 07613327057041 | 90-S Accelerator, Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327057034 | 90-S Cruise, Suction Probe, Non-bendable, Max Cut Level 1 |
| 07613327057027 | 90-S Max, Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327056990 | 50-S XL Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327056983 | 50-S Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327056976 | 90-S XL Probe, Suction, Non-bendable, Max Cut Level 11 |
| 07613327056969 | 30-S Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327056952 | 90-S, Suction Probe, Non-bendable, Max Cut Level 11 |
| 07613327056945 | Hook XL Probe, Non-suction, Bendable, Max Cut Level 7 |
| 07613327056938 | Hook Probe, Non-suction, Bendable, Max Cut Level 7 |
| 07613327056921 | Direct Probe, Non-suction, Bendable, Max Cut Level 6 |
| 07613327056914 | Lateral Probe, Non-suction, Bendable, Max Cut Level 8 |
| 07613327056907 | Contour Probe, Non-suction, Bendable, Max Cut Level 7 |
| 07613327056884 | Aardvark, Suction Probe, Bendable, Max Cut Level 6 |
| 07613327056877 | Micro-Claw, Small-Joint Probe, Non-suction, Bendable, Max Cut Level 6 |
| 07613327056860 | Micro-Brush, Small-Joint Probe, Non-suction, Bendable, Max Cut Level 6 |