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Curaplex

FDA UDI

Class II (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
ADVANCED TRAUMA KIT - US EMBASSY FDA UDI
Model / Reference
660222 FDA UDI
Description
ADVANCED TRAUMA KIT - US EMBASSY FDA UDI

Identifiers

Primary DI / UDI-DI
00815277021234 FDA UDI
FDA Product Code
DQA FDA UDI
MHC FDA UDI
FOZ FDA UDI
BTM FDA UDI
POQ FDA UDI
HEB FDA UDI
FRO FDA UDI
FMF FDA UDI
DXQ FDA UDI
MMK FDA UDI
NBW FDA UDI
GAR FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
880.5570 FDA UDI
880.5200 FDA UDI
868.5915 FDA UDI
880.5440 FDA UDI
884.5470 FDA UDI
880.5860 FDA UDI
870.1120 FDA UDI
862.1345 FDA UDI
878.5020 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 II — 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

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI 448caea0-125a-4aab-be08-c8559e6d150e 33 fields · synced May 30, 2026