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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
Capnography oxygen mask FDA UDI
Device Name
MASK,PrO2,OX,ADL,HI.CONC,ETCO2,30/BX FDA UDI
Model / Reference
301-PrO2LT-0 FDA UDI
Description
MASK,PrO2,OX,ADL,HI.CONC,ETCO2,30/BX FDA UDI

Identifiers

Catalog Number
301-PrO2LT-0 FDA UDI
Primary DI / UDI-DI
00810094574864 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Capnography oxygen mask FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capnography oxygen mask

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

Similar devices

Also classified as Capnography oxygen mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e65db36-a2b0-4cd4-85b3-5cc0a00a1c96 35 fields · synced Jun 8, 2026