0306813000

GUDID 37613327374446

HAND DRILL

STRYKER CORPORATION

Manual surgical rotary handpiece

• Primary Device ID: 37613327374446
• NIH Device Record Key: 97c97396-600b-469f-8a7d-51529eff5768
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0306813000
• Catalog Number: 0306813000
• 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

Customer Support Contacts

• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com
• Phone: +1(800)253-3210
• Email: inst.stryker.cs@stryker.com

Device Dimensions

• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge
• Needle Gauge: 13 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327374445 [Primary]
GS1	37613327374446 [Package]; Contains: 07613327374445; Package: pack [6 Units]; In Commercial Distribution

FDA Product Code

• OCJ: spinal channeling instrument, vertebroplasty

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-05-07
• Device Publish Date: 2018-04-04

Devices Manufactured by STRYKER CORPORATION

• 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