E+R

GUDID 06975871430369

DOUBLE HEAD STETHOSCOPE PURPLE

Wenzhou Caretek Medical Device Co., Ltd.

Mechanical stethoscope

• Primary Device ID: 06975871430369
• NIH Device Record Key: 8c1c67a1-552a-4aff-8039-d9ac04c473ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E+R
• Version Model Number: 143231
• Company DUNS: 527815967
• Company Name: Wenzhou Caretek Medical Device 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: 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	06975871430369 [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: 2024-03-21
• Device Publish Date: 2024-03-13

On-Brand Devices [E+R]

• 06975871430376: DOUBLE HEAD STETHOSCOPE PINK
• 06975871430369: DOUBLE HEAD STETHOSCOPE PURPLE
• 06975871430352: DOUBLE HEAD STETHOSCOPE YELLOW