← Back to catalogue

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
Suction oesophageal intubation detector, adult FDA UDI
Device Name
LA Rescue ALS Airway Kit - Red FDA UDI
Model / Reference
EMP4000RC FDA UDI
Description
LA Rescue ALS Airway Kit - Red FDA UDI

Identifiers

Primary DI / UDI-DI
00851772007083 FDA UDI
FDA Product Code
HTD FDA UDI
PHS FDA UDI
FMF FDA UDI
BTR FDA UDI
OGH FDA UDI
GMDN Term
Suction oesophageal intubation detector, adult FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
868.5110 FDA UDI
880.5860 FDA UDI
868.5730 FDA UDI
868.5540 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: Blood pressure cuff, single-useAirway tube forceps, single-useSuction oesophageal intubation detector, adult

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 Suction oesophageal intubation detector, adult.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Emergency Medical Products, Inc.

Sources (1)

  • FDA UDI 68f50ad5-3093-4b30-8936-cefdf115a593 33 fields · synced Jun 8, 2026