Identity
- Trade Name
- ViaMed FDA UDI
- Generic Name
- Mechanical external stethoscope FDA UDI
- Device Name
- Chest piece with two functions. The binaural head frame is made seamless brass tubes. Thick walled 22" PVC tubing, durable and noise proof. Comfortable smooth plastic ear plugs. Mixed Colors. FDA UDI
- Model / Reference
- 13410-MIX FDA UDI
- Description
- Chest piece with two functions. The binaural head frame is made seamless brass tubes. Thick walled 22" PVC tubing, durable and noise proof. Comfortable smooth plastic ear plugs. Mixed Colors. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00811382011467 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
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Mechanical external stethoscope
ViaMed by Rece International Corp. — 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
- Rece International Corp.
Sources (1)
- FDA UDI 14a2ead5-5906-4c67-b5ee-b81e66d69d1b 34 fields · synced Jun 1, 2026