0306703000

GUDID 37613327051286

ACM w/ nozzle restr/press

STRYKER CORPORATION

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 37613327051286
• NIH Device Record Key: 63c4a485-bc56-4a1e-a0bf-658a11670855
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0306703000
• Catalog Number: 0306703000
• 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327051285 [Primary]
GS1	37613327051286 [Package]; Contains: 07613327051285; Package: pack [6 Units]; In Commercial Distribution

FDA Product Code

• LZN: CEMENT OBTURATOR

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-24

Devices Manufactured by STRYKER CORPORATION

• 07613327261820 - MAC: 2024-10-29 SCREWDRIVER
• 07613327271089 - DYNATRAN: 2024-10-29 COMPRESSOR
• 07613327273885 - Aero-LL: 2024-10-29 INSERTER - DISTRACTOR
• 37613327566162 - Neptune: 2024-10-23 V2 SPECIMEN COLLECTION MANIFOLD KIT
• 07613327578577 - Target Tetra: 2024-10-08 Detachable Coil
• 07613327578584 - Target Tetra: 2024-10-08 Detachable Coil
• 07613327578591 - Target Tetra: 2024-10-08 Detachable Coil
• 07613327578607 - Target Tetra: 2024-10-08 Detachable Coil