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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
Curaplex ALS Pedi Kit For University Hosp of Cleveland FDA UDI
Model / Reference
2525-16050 FDA UDI
Description
Curaplex ALS Pedi Kit For University Hosp of Cleveland FDA UDI

Identifiers

Primary DI / UDI-DI
00815277020633 FDA UDI
FDA Product Code
FMF FDA UDI
MMK FDA UDI
DRX FDA UDI
DXQ FDA UDI
BTM FDA UDI
FPB FDA UDI
CCK FDA UDI
GJE FDA UDI
POQ FDA UDI
FHM FDA UDI
BTR FDA UDI
PEZ FDA UDI
FMI FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
880.5570 FDA UDI
870.2360 FDA UDI
870.1120 FDA UDI
868.5915 FDA UDI
880.5440 FDA UDI
868.1400 FDA UDI
862.1675 FDA UDI
878.4800 FDA UDI
868.5730 FDA UDI
880.5200 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 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 bac900c9-c23a-484b-9ffc-fe4a33f37c4f 33 fields · synced May 30, 2026