Rhino Rescue

GUDID 06970784670222

wenzhou dongfang medical instrument co.,ltd

Mechanical external stethoscope

• Primary Device ID: 06970784670222
• NIH Device Record Key: 32ae89de-8554-4ab8-8a73-bbf03454d9ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rhino Rescue
• Version Model Number: KT-101
• Company DUNS: 529870243
• Company Name: wenzhou dongfang medical instrument co.,ltd
• 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: true
• Expiration Date: true
• 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	06970784670222 [Primary]

FDA Product Code

• LDE: Stethoscope, Manual

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: 2026-04-01
• Device Publish Date: 2026-03-24

Devices Manufactured by wenzhou dongfang medical instrument co.,ltd

• 06970784670222 - Rhino Rescue: 2026-04-01
• 06970784670222 - Rhino Rescue: 2026-04-01
• 06970784670192 - NA: 2024-09-17
• 06970784670178 - NA: 2024-08-28
• 06970784670185 - NA: 2024-08-28
• 06970784670130 - NA: 2024-05-14
• 06970784670147 - NA: 2024-05-14
• 06970784670154 - NA: 2024-05-14
• 06970784670161 - NA: 2024-05-14