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ViaMed

FDA UDI

Class I (US FDA UDI)

by Rece International Corp.

Identity

Trade Name
ViaMed FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
High acoustical quality. Heavy-walled 22" tubing. Latex Free. Includes five-in-one accessory kit. Two extra pair of soft ear tips. Color Blue. FDA UDI
Model / Reference
13411-BLUE FDA UDI
Description
High acoustical quality. Heavy-walled 22" tubing. Latex Free. Includes five-in-one accessory kit. Two extra pair of soft ear tips. Color Blue. FDA UDI

Identifiers

Primary DI / UDI-DI
00811382011498 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

No

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

Similar devices

Also classified as Mechanical external stethoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f54c6137-7731-408b-a945-b2fda47d3e4a 34 fields · synced Jun 6, 2026