← Back to catalogue

Welch Allyn Harvey Stethoscope

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5079-322SModel 901039

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn Harvey Stethoscope EUDAMED
Welch Allyn, Inc. FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
Welch Allyn Harvey DLX Cardiology Stethoscope with Stainless Steel Triple-Head Chestpiece (Low-Frequency Bell, Adult Diaphragm, and Pediatric Diaphragm), Dual Lumen Latex-Free Tubing, Harvey Heart Sounds CD, Harvey DLX Accessory Kit (#5079-315); 28 in/71.1 cm; Burgundy FDA UDI
Model / Reference
901039 EUDAMEDFDA UDI
5079-322S EUDAMED
Description
Welch Allyn Harvey DLX Cardiology Stethoscope with Stainless Steel Triple-Head Chestpiece (Low-Frequency Bell, Adult Diaphragm, and Pediatric Diaphragm), Dual Lumen Latex-Free Tubing, Harvey Heart Sounds CD, Harvey DLX Accessory Kit (#5079-315); 28 in/71.1 cm; Burgundy FDA UDI

Identifiers

Catalog Number
5079-322S FDA UDI
Primary DI / UDI-DI
00732094115086 EUDAMEDFDA UDI
Basic UDI-DI
0732094GMN901039F9 EUDAMED
FDA Product Code
LDE FDA UDI
EMDN Code
C9005 PHONENDOSCOPES AND STETHOSCOPES EUDAMED
GMDN Term
Mechanical external stethoscope FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
870.1875 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Welch Allyn Harvey Stethoscope by Welch Allyn, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Welch Allyn, Inc.
EUDAMED SRN
US-MF-000013394
Authorised Representative
Welch Allyn Limited IE-AR-000000768

Sources (2)

  • EUDAMED 2c59e8d3-2b24-45ea-b659-f5e92d376aa6 61 fields · synced Jun 20, 2026
  • FDA UDI 145c4863-c55f-4365-abc1-efbe27349590 35 fields · synced May 29, 2026