E5 eyevan

GUDID 04582669003241

EYEVAN INC.

Spectacle frame

• Primary Device ID: 04582669003241
• NIH Device Record Key: dae509a1-c5d4-41ef-8750-894b085ce48c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E5 eyevan
• Version Model Number: C1 45 BKWG
• Company DUNS: 705184505
• Company Name: EYEVAN INC.
• 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: false
• 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	04582669003241 [Primary]

FDA Product Code

• HQZ: Frame, Spectacle

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: 2024-11-08
• Device Publish Date: 2024-10-31

On-Brand Devices [E5 eyevan]

• 04582669015794: P15R-E 48 BL
• 04582669015787: P15R-E 48 SB2
• 04582669015770: P15R-E 48 MBK
• 04582669015763: P15R-E 48 MBK
• 04582669015756: P15R-E 48 BK
• 04582669015749: P14R-E 47 BC
• 04582669015732: P14R-E 47 SB2
• 04582669015725: P14R-E 47 BRH
• 04582669015718: P14R-E 47 DM
• 04582669015701: P14R-E 47 BK
• 04582669003432: M8 48 AG
• 04582669003425: M8 48 ST
• 04582669003418: M8 48 WG
• 04582669003401: M8 48 MBRWGWG
• 04582669003395: M8 48 MBKWGWG
• 04582669003388: C3 48 BLWG
• 04582669003371: C3 48 MBKST
• 04582669003364: C3 48 DMWG
• 04582669003357: C3 48 BKWG
• 04582669003340: C3 48 BKST
• 04582669003289: C1 45 RUWG
• 04582669003272: C1 45 SMKWG
• 04582669003265: C1 45 SPAWG
• 04582669003258: C1 45 DMWG
• 04582669003241: C1 45 BKWG