Jamar

GUDID 00087453152104

Jamar Finger Goniometer 2° increment scale (081275676)

HYGENIC CORPORATION, THE

Manual goniometer

• Primary Device ID: 00087453152104
• NIH Device Record Key: 474ca213-c56a-4733-830a-9b1ed86b2a17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jamar
• Version Model Number: 15210
• Company DUNS: 004163390
• Company Name: HYGENIC CORPORATION, THE
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00087453152104 [Primary]
GS1	10087453152101 [Package]; Package: [1 Units]; In Commercial Distribution

FDA Product Code

• KQW: Goniometer, Nonpowered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2025-03-17
• Device Publish Date: 2023-12-07

On-Brand Devices [Jamar]

• 10885914030445: Jamar Finger Goniometer 2° increment scale (081275676)
• 00087453152104: Jamar Finger Goniometer 2° increment scale (081275676)