NECKLITE

GUDID 08057592700131

FLAMOR SRL

Cervical spine collar, reusable

• Primary Device ID: 08057592700131
• NIH Device Record Key: 4184d84a-12c0-4f2c-814c-b16c28eed002
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NECKLITE
• Version Model Number: BLK
• Company DUNS: 629852208
• Company Name: FLAMOR SRL
• Device Count: 1
• DM Exempt: true
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08057592700131 [Primary]

FDA Product Code

• IQF: Orthosis, Cervical-Thoracic, Rigid

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: 2025-02-04
• Device Publish Date: 2025-01-27

On-Brand Devices [NECKLITE]

• 08057592700148: BLK / SC
• 08057592700131: BLK
• 08057592700124: YLW / SC
• 08057592700117: YLW
• 08057592700100: BLUE / SC
• 08057592700094: BLUE