n.a 20161220

GUDID 04048551317488

LED Nova 150, without accessories

Karl Storz GmbH & Co. KG

Endoscopic light source unit, line-powered

• Primary Device ID: 04048551317488
• NIH Device Record Key: c5df8104-ec53-4f9c-b52c-cdf8526d7007
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: n.a
• Version Model Number: 20161220
• Catalog Number: 20161220
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• 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: true
• 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	04048551317488 [Primary]

FDA Product Code

• NTN: Led light source

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: 2024-12-09
• Device Publish Date: 2024-11-29

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• 04048551360460 - n.a.: 2024-12-23 Nitinol Guide Wire Ø 1.1 mm, 38.5 cm
• 04048551360484 - n.a.: 2024-12-23 Nitinol Guide Wire Ø 2 mm, 38.5 cm
• 04048551364437 - n.a.: 2024-12-23 Guide Sleeve, short, 10.5 cm
• 04048551364444 - n.a.: 2024-12-23 Guide Sleeve, long, 14.5 cm
• 04048551415320 - n.a.: 2024-12-20 KARL STORZ AIDA