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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
KIT NEW USSS F.A.T. KIT (7/2002) FDA UDI
Model / Reference
NSS2003N FDA UDI
Description
KIT NEW USSS F.A.T. KIT (7/2002) FDA UDI

Identifiers

Primary DI / UDI-DI
00815277022804 FDA UDI
FDA Product Code
BTA FDA UDI
CAN FDA UDI
OEV FDA UDI
OKH FDA UDI
CBP FDA UDI
BTL FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
868.2700 FDA UDI
868.5915 FDA UDI
878.4040 FDA UDI
868.5870 FDA UDI
868.5925 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 0c6663f5-a456-4cec-96d5-48e48f27254b 33 fields · synced May 30, 2026