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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
In-line CPAP set, nebulizing FDA UDI
Device Name
*Custom* Memphis AeroEclipse Mask SM FDA UDI
Model / Reference
8600-AEMSKP-1486 FDA UDI
Description
*Custom* Memphis AeroEclipse Mask SM FDA UDI

Identifiers

Primary DI / UDI-DI
00815277022446 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
In-line CPAP set, nebulizing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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: In-line CPAP set, nebulizing

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

Similar devices

Also classified as In-line CPAP set, nebulizing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4728f2d2-5b6b-4373-acf3-141d03ae4e36 33 fields · synced Jun 8, 2026