Pack of 6 pcs. ri-pen® 5071

GUDID 04045396006959

The Riester diagnostic light is used for ophthalmological examination.

Rudolf Riester GmbH

Hand-held examination/treatment light Hand-held examination/treatment light Hand-held examination/treatment light Hand-held examination/treatment light Hand-held examination/treatment light Hand-held examination/treatment light Hand-held examination/treatment light

• Primary Device ID: 04045396006959
• NIH Device Record Key: d70cd3ac-c4a1-4500-a3b8-19e37c7b2f7a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pack of 6 pcs. ri-pen®
• Version Model Number: 5071
• Catalog Number: 5071
• Company DUNS: 537208717
• Company Name: Rudolf Riester GmbH
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04045396006959 [Primary]

FDA Product Code

• KYT: Light, Examination, Medical, Battery Powered

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: 2021-07-27
• Device Publish Date: 2021-07-19

On-Brand Devices [Pack of 6 pcs. ri-pen®]

• 04045396006959: The Riester diagnostic light is used for ophthalmological examination.
• 04045396006942: The Riester diagnostic light is used for ophthalmological examination.