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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
Atomizing surgical topical solution applicator FDA UDI
Device Name
Curaplex Opioid Training Kit FDA UDI
Model / Reference
670050-KIT FDA UDI
Description
Curaplex Opioid Training Kit FDA UDI

Identifiers

Catalog Number
670050-KIT FDA UDI
Primary DI / UDI-DI
00815277021517 FDA UDI
FDA Product Code
FOZ FDA UDI
CCT FDA UDI
GMDN Term
Atomizing surgical topical solution applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
868.5170 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: Atomizing surgical topical solution applicator

Curaplex by Bound Tree Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Atomizing surgical topical solution applicator.

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 a494521f-c4d3-4d23-8853-5fb3b1f9ab9a 34 fields · synced May 31, 2026