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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
First aid kit, medicated FDA UDI
Device Name
X Pouch - Tactical Black FDA UDI
Model / Reference
EMPXT FDA UDI
Description
X Pouch - Tactical Black FDA UDI

Identifiers

Primary DI / UDI-DI
00851772007175 FDA UDI
FDA Product Code
OVR FDA UDI
LMG FDA UDI
OPA FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
878.4490 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

Yes

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, medicatedAneroid manual sphygmomanometerCardiopulmonary resuscitation kit, reusablePlant polysaccharide haemostatic agent, non-bioabsorbable, antimicrobial

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 Plant polysaccharide haemostatic agent, non-bioabsorbable, antimicrobial.

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 03d9b331-a0b9-4c86-b103-7d2ea15d3946 33 fields · synced May 30, 2026