Curaplex

FDA UDI

Class I (US FDA UDI)

by Emergency Medical Products, Inc.

Identity

Trade Name: Curaplex FDA UDI
Generic Name: First aid kit, non-medicated, reusable FDA UDI
Device Name: *Custom* Lycoming County Public IFAK Advanced FDA UDI
Model / Reference: 8600-01405 FDA UDI
Description: *Custom* Lycoming County Public IFAK Advanced FDA UDI

Identifiers

Catalog Number: 8600-01405 FDA UDI
Primary DI / UDI-DI: 00851772007335 FDA UDI
FDA Product Code: OHO FDA UDI
GMDN Term: First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 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

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: First aid kit, non-medicated, reusable

Curaplex 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 6757ac7f-2db8-4539-8115-c54024b3b2e2 34 fields · synced Jun 1, 2026