Shin Splint GNK03-S

GUDID 00810006681819

Shin Splint - Small

PRIMO INC

Compression/pressure sock/stocking, single-use

• Primary Device ID: 00810006681819
• NIH Device Record Key: cafee61a-1cd1-4452-a5f9-b1c314835987
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shin Splint
• Version Model Number: GNK03-S
• Catalog Number: GNK03-S
• Company DUNS: 958758146
• Company Name: PRIMO 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: true
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810006681819 [Primary]

FDA Product Code

• ILH: Splint, Hand, And Components

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-10-07
• Device Publish Date: 2019-02-27

On-Brand Devices [Shin Splint ]

• 00810006681826: Shin Splint - XLarge
• 00810006681819: Shin Splint - Small
• 00810006681802: Shin Splint - Medium
• 00810006681796: Shin Splint - Large