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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
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Curaplex Slct IV Admin Set, 15Dp,89in,Rlr Clmp,PP Ysite,Sr-Lk NdleFr Y, Attch Ext Set, 1/EA 50EA/CS FDA UDI
Model / Reference
1712-60830 FDA UDI
Description
Curaplex Slct IV Admin Set, 15Dp,89in,Rlr Clmp,PP Ysite,Sr-Lk NdleFr Y, Attch Ext Set, 1/EA 50EA/CS FDA UDI

Identifiers

Catalog Number
1712-60830 FDA UDI
Primary DI / UDI-DI
00812277034493 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Basic intravenous administration set, noninvasive

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

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

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 9927a8b3-26cf-4a55-bd9b-30948418e599 34 fields · synced May 31, 2026