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: Blood pressure cuff, single-use FDA UDI
Device Name: First Call-in Bag Junior FDA UDI
Model / Reference: LA8641R FDA UDI
Description: First Call-in Bag Junior FDA UDI

Identifiers

Primary DI / UDI-DI: 00851772007205 FDA UDI
FDA Product Code: IMD FDA UDI
OVR FDA UDI
OPA FDA UDI
MCY FDA UDI
DXQ FDA UDI
LDE FDA UDI
GMDN Term: Blood pressure cuff, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5710 FDA UDI
878.4014 FDA UDI
880.5075 FDA UDI
870.1120 FDA UDI
870.1875 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: First aid kit, medicated Mechanical external stethoscope Blood pressure cuff, single-use

Emergency Medical Products by Emergency Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Emergency Medical Products, Inc.

Sources (1)

FDA UDI e3982d22-3531-4fdb-9da9-4b848bd138d7 33 fields · synced May 30, 2026