Joint Jack Company 1455

GUDID 00858534005141

Joint Jack Company

Pressure bandage, non-latex, single-use

• Primary Device ID: 00858534005141
• NIH Device Record Key: ceaa5ed2-16fd-427b-a139-f90a3dcade2d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Joint Jack Company
• Version Model Number: Hand Wrap 2"
• Catalog Number: 1455
• Company DUNS: 085068021
• Company Name: Joint Jack Company
• 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: 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	00858534005141 [Primary]

FDA Product Code

• FQM: Bandage, Elastic

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: 2024-01-24
• Device Publish Date: 2024-01-16

On-Brand Devices [Joint Jack Company]

• 00858534005004: Joint Jack Splint- small
• 00858534005172: Hand Wrap 6"
• 00858534005165: Hand Wrap 4"
• 00858534005158: Hand Wrap 3"
• 00858534005141: Hand Wrap 2"
• 00858534005127: Dystrophile
• 00858534005110: Joint Cinch Strap
• 00858534005073: Joint-Spring 11"
• 00858534005066: Joint-Spring 9"
• 00858534005059: Joint-Spring 7"
• 00858534005042: Joint Jack Splint- extra extra large
• 00858534005035: Joint Jack Splint- extra large
• 00858534005028: Joint Jack Splint- large
• 00858534005011: Joint Jack Splint- medium