Sirca CG 3913175

GUDID 07613327616644

Berchtold Holding GmbH

Fixed examination/treatment room light

• Primary Device ID: 07613327616644
• NIH Device Record Key: ba9a840b-14df-470f-bed2-c77d904e3757
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sirca
• Version Model Number: CG3913175
• Catalog Number: CG 3913175
• Company DUNS: 316153824
• Company Name: Berchtold Holding 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: false
• Serial Number: true
• Manufacturing Date: false
• 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	07613327616644 [Primary]

FDA Product Code

• KZF: Device, medical examination, ac 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: 2023-07-24
• Device Publish Date: 2023-07-14

On-Brand Devices [Sirca]

• 07613327622706: Stryker Examination Light Sirca ? Ceiling Mounted
• 07613327616644: CG3913175
• 07613327616620: CG3913275
• 07613327616569: CF3893075
• 07613327616545: Stryker Examination Light ? Ceiling Mounted