VALVESAFE

GUDID 05060602250017

VALVESAFE

MEDITECH ENDOSCOPY LTD

Device sterilization/disinfection container, single-use

• Primary Device ID: 05060602250017
• NIH Device Record Key: 539470c4-9d44-45c7-a439-fc291672dca4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VALVESAFE
• Version Model Number: INOV8-001
• Company DUNS: 219397009
• Company Name: MEDITECH ENDOSCOPY LTD
• Device Count: 100
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060602250017 [Unit of Use]
GS1	15060602250014 [Primary]

FDA Product Code

• FFY: Adaptor, Bulbs, Miscellaneous, For Endoscope

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: 2023-09-01
• Device Publish Date: 2023-08-24

Devices Manufactured by MEDITECH ENDOSCOPY LTD

• 05060602250307 - Protech S: 2026-02-09 ENDOSCOPIC STORAGE COVER
• 05060602250543 - Protech XL: 2026-02-09 ENDOSCOPIC STORAGE COVER
• 05060602250291 - Protech L: 2026-02-05 ENDOSCOPIC STORAGE COVER
• 05060602250024 - ECO EZ CLEANSE: 2023-09-04 ECO EZ CLEANSE
• 05060602250017 - VALVESAFE: 2023-09-01VALVESAFE
• 05060602250017 - VALVESAFE: 2023-09-01 VALVESAFE