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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
KIT, RAPID RESPONSE AIR - RRAK FDA UDI
Model / Reference
2525-36703 FDA UDI
Description
KIT, RAPID RESPONSE AIR - RRAK FDA UDI

Identifiers

Primary DI / UDI-DI
00815277027465 FDA UDI
FDA Product Code
OGI FDA UDI
BZT FDA UDI
CCK FDA UDI
CAN FDA UDI
DQA FDA UDI
OGH FDA UDI
LNZ FDA UDI
KGB FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 FDA UDI
868.1920 FDA UDI
868.1400 FDA UDI
868.2700 FDA UDI
870.2700 FDA UDI
868.5540 FDA UDI
868.5730 FDA UDI
868.5570 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

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI cb98e832-48d2-4010-ac4e-3ed96a2028d7 33 fields · synced May 31, 2026