0300040000

GUDID 34546540898563

Bucket Liners

STRYKER CORPORATION

Bucket liner

• Primary Device ID: 34546540898563
• NIH Device Record Key: 20bf08ba-2429-4b8b-87a9-3c10b84c263a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0300040000
• Catalog Number: 0300040000
• 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: false
• Lot Batch: false
• 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540898562 [Primary]
GS1	34546540898563 [Package]; Contains: 04546540898562; Package: pack [100 Units]; In Commercial Distribution

FDA Product Code

• LGG: INSTRUMENT, CAST APPLICATION/REMOVAL, MANUAL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-25
• Device Publish Date: 2018-09-24

Devices Manufactured by STRYKER CORPORATION

• 07613327419252 - Patient Helper: 2024-12-23
• 37613327556651 - Neptune: 2024-12-23 SafeAir 125mm Suction Sleeve, Non-Sterile
• 07613327643879 - Iconix: 2024-12-19 Iconix DC Guide for 2.3mm Anchor
• 07613327643886 - Iconix: 2024-12-19 Iconix DC Obturator for 2.3 Anchor
• 07613327644067 - Neptune: 2024-12-16 V2 SPECIMEN COLLECTION MANIFOLD
• 07613327262469 - VBOSS: 2024-12-10 ENDPLATE TIP SMALL
• 07613327262483 - VBOSS: 2024-12-10 ENDPLATE TIP LARGE
• 07613327262506 - VBOSS: 2024-12-10 ENDPLATE TIP OFFSET