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Emergency Medical Products

FDA UDI

Class I (US FDA UDI)

by Emergency Medical Products, Inc.

Identity

Trade Name
Emergency Medical Products FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
O2 To Go Pro Trauma Kit FDA UDI
Model / Reference
EMP3250RC FDA UDI
Description
O2 To Go Pro Trauma Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00851772007236 FDA UDI
FDA Product Code
FMC FDA UDI
DXQ FDA UDI
HTD FDA UDI
IMD FDA UDI
LDE FDA UDI
PHS FDA UDI
CAN FDA UDI
NOC FDA UDI
MCY FDA UDI
GAX FDA UDI
BTM FDA UDI
BYG FDA UDI
GMDN Term
Mechanical external stethoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
870.1120 FDA UDI
878.4800 FDA UDI
890.5710 FDA UDI
870.1875 FDA UDI
868.5110 FDA UDI
868.2700 FDA UDI
878.3910 FDA UDI
880.5075 FDA UDI
878.5900 FDA UDI
868.5915 FDA UDI
868.5580 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: First aid kit, medicatedMechanical external stethoscope

Emergency Medical Products by Emergency Medical Products, Inc. — 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

Manufacturer
Emergency Medical Products, Inc.

Sources (1)

  • FDA UDI cb797eeb-2ca0-4e15-83b7-558b683e6cda 33 fields · synced May 30, 2026