← Back to catalogue

Curaplex

FDA UDI

Class II (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Microbial medical gas filter, single-use FDA UDI
Device Name
TRANSPORT VENTILATOR CIRCUIT,BACTERIAL/VIRAL FILTER,9 FT EXPANDABLE CORRAGATED TUBING FDA UDI
Model / Reference
1004SPCOF FDA UDI
Description
TRANSPORT VENTILATOR CIRCUIT,BACTERIAL/VIRAL FILTER,9 FT EXPANDABLE CORRAGATED TUBING FDA UDI

Identifiers

Catalog Number
301-1004SPCOF FDA UDI
Primary DI / UDI-DI
00810071636448 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Microbial medical gas filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

Yes

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Microbial medical gas filter, single-use

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

Similar devices

Also classified as Microbial medical gas filter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 973ea862-67cf-444e-a976-1f847ba7ccea 34 fields · synced Jun 8, 2026