| Primary Device ID | 04546540075222 |
| NIH Device Record Key | 599aabb9-9a6f-4d64-a266-b24c712a949c |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5100020200 |
| Catalog Number | 5100020200 |
| 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 | false |
| 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(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540075222 [Primary] |
| DZI | DRILL, BONE, POWERED |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
[04546540075222]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-20 |
| Device Publish Date | 2016-09-23 |
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| 07613327273243 - TRIO + | 2025-01-03 FLEXIBLE EXTENDER II |