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Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
First aid kit, non-medicated, reusable FDA UDI
Device Name
*Custom* FBI SWAT Medic Kit FDA UDI
Model / Reference
660448-QC FDA UDI
Description
*Custom* FBI SWAT Medic Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00815277027700 FDA UDI
FDA Product Code
KGZ FDA UDI
BTM FDA UDI
OQU FDA UDI
CBP FDA UDI
OGK FDA UDI
PEZ FDA UDI
FMF FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
868.5915 FDA UDI
868.5730 FDA UDI
868.5870 FDA UDI
868.1400 FDA UDI
880.5200 FDA UDI
880.5860 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, non-medicated, reusable

Curaplex by Bound Tree Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3303f4f0-8f50-4e81-b3e6-dac3573113bb 33 fields · synced May 30, 2026