Therabath

GUDID 00702173122755

WR MEDICAL ELECTRONICS CO INC

Physical therapy paraffin wax bath

• Primary Device ID: 00702173122755
• NIH Device Record Key: be03fa65-b6c5-419b-a831-03b6dd09402c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Therabath
• Version Model Number: TB9
• Company DUNS: 006196604
• Company Name: WR MEDICAL ELECTRONICS CO 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: 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	00702173122755 [Primary]

FDA Product Code

• IMC: Bath, Paraffin

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: 2020-03-19
• Device Publish Date: 2020-03-11

On-Brand Devices [Therabath]

• 00702173123226: TB7
• 00702173123202: TB6
• 00702173122809: TB10
• 00702173122755: TB9