Identity
- Trade Name
- Strong Manufacturers FDA UDI
- Generic Name
- Mechanical external stethoscope FDA UDI
- Device Name
- Manual stethoscope used to project the sounds associated with the heart, arteries, veins and other internal organs. Single head, yellow, not made with natural rubber latex. Case of 25 each. FDA UDI
- Model / Reference
- 7101 FDA UDI
- Description
- Manual stethoscope used to project the sounds associated with the heart, arteries, veins and other internal organs. Single head, yellow, not made with natural rubber latex. Case of 25 each. FDA UDI
Identifiers
- Catalog Number
- 7101 FDA UDI
- Primary DI / UDI-DI
- 00850040791174 FDA UDI
- FDA Product Code
- LDE FDA UDI
- GMDN Term
- Mechanical external stethoscope FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.1875 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Mechanical external stethoscope
Strong Manufacturers by Strong Medical Partners LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Proscope™ — American Diagnostic Corporation · Class I
- Adscope® — American Diagnostic Corporation · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Strong Medical Partners LLC
Sources (1)
- FDA UDI 2dd5f1d5-3b9f-42df-9a40-0e6e985ac30a 36 fields · synced May 31, 2026