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Curaplex

FDA UDI

Class II (US FDA UDI)

by Tri-Anim Health Services, Inc.

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Pleural drainage system FDA UDI
Device Name
HANDLE,SUCTION,YANKAUER,STRAIGHT TIP,W/O CONTROL VENT,STERILE 50/CA FDA UDI
Model / Reference
301-005-10010 FDA UDI
Description
HANDLE,SUCTION,YANKAUER,STRAIGHT TIP,W/O CONTROL VENT,STERILE 50/CA FDA UDI

Identifiers

Primary DI / UDI-DI
00812574025064 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Pleural drainage system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Pleural drainage system

Curaplex by Tri-Anim Health Services, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleural drainage system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tri-Anim Health Services, Inc.

Sources (1)

  • FDA UDI 624b7605-8f14-4e2c-bac4-e1d98cd9c86c 33 fields · synced May 30, 2026