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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
Airway tube forceps, single-use FDA UDI
Device Name
LA Rescue ALS Airway Kit - Royal Blue FDA UDI
Model / Reference
EMP4000RBC FDA UDI
Description
LA Rescue ALS Airway Kit - Royal Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00851772007076 FDA UDI
FDA Product Code
HTD FDA UDI
FMF FDA UDI
BTR FDA UDI
OGH FDA UDI
PHS FDA UDI
GMDN Term
Airway tube forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
880.5860 FDA UDI
868.5730 FDA UDI
868.5540 FDA UDI
868.5110 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

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Manufacturer

Manufacturer
Emergency Medical Products, Inc.

Sources (1)

  • FDA UDI b3631fac-4829-452b-9162-a5eb42c61061 33 fields · synced Jun 8, 2026