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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
Curaplex Med-E-Pack 3 - Refill Pak FDA UDI
Model / Reference
660488 FDA UDI
Description
Curaplex Med-E-Pack 3 - Refill Pak FDA UDI

Identifiers

Primary DI / UDI-DI
00815277027724 FDA UDI
FDA Product Code
OJS FDA UDI
MCY FDA UDI
KYP FDA UDI
OHO FDA UDI
OKO FDA UDI
DXQ FDA UDI
OJJ FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
880.5075 FDA UDI
880.5740 FDA UDI
878.4014 FDA UDI
878.4683 FDA UDI
870.1120 FDA UDI
878.4022 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

No

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

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI 64034581-1936-4406-85c4-8ab122e40e03 33 fields · synced Jun 1, 2026