Hemopore 5400-222-208S

GUDID 37613327500487

STRYKER CORPORATION

ENT space-occupying dressing, animal-derived

• Primary Device ID: 37613327500487
• NIH Device Record Key: e5788d0d-8f93-4ca9-8962-a9adbf74e93e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hemopore
• Version Model Number: 5400222208S
• Catalog Number: 5400-222-208S
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327500486 [Primary]
GS1	37613327500487 [Package]; Contains: 07613327500486; Package: pack [2 Units]; In Commercial Distribution

FDA Product Code

• LYA: SPLINT, INTRANASAL SEPTAL

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: 2020-01-16
• Device Publish Date: 2020-01-08

On-Brand Devices [Hemopore]

• 37613327117234: 5400020208
• 37613327500487: 5400222208S