GUDID 04250480106143

Sealing cap laser channel UMP, 10 pieces

SCHÖLLY FIBEROPTIC GmbH

Endoscope channel support kit

• Primary Device ID: 04250480106143
• NIH Device Record Key: e1b9ea89-b4df-4766-9272-c502129e4808
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 41.0678a
• Company DUNS: 316276682
• Company Name: SCHÖLLY FIBEROPTIC GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: 9999999999
• Email: info@schoelly-usa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250480106143 [Primary]

FDA Product Code

• FGA: Kit, Nephroscope

Sterilization

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

[04250480106143]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-28
• Device Publish Date: 2020-04-20

Devices Manufactured by SCHÖLLY FIBEROPTIC GmbH

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• 04250480100356 - NA: 2025-01-23 Adapter light guide, Wolf Endoscope
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