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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
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
*SEE NOTES* Curaplex Capnography ETCO2 Sampling Lines w/Airway Adapter Multipack (incl 5 #301-5107ET FDA UDI
Model / Reference
670271-KIT FDA UDI
Description
*SEE NOTES* Curaplex Capnography ETCO2 Sampling Lines w/Airway Adapter Multipack (incl 5 #301-5107ET FDA UDI

Identifiers

Catalog Number
670271-KIT FDA UDI
Primary DI / UDI-DI
00810094579418 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling 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

No

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

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: Nasal oxygen cannula, carbon-dioxide-sampling

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

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e7aedfa8-64c3-4085-89b6-274a784a72cc 34 fields · synced May 30, 2026