← Back to catalogue

Curaplex

FDA UDI

Class II (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Peripheral intravenous catheterization support kit FDA UDI
Device Name
Curaplex IV Start Kit w/ Tegaderm, Skin Prep, Ext Set, Flush FDA UDI
Model / Reference
670063-KIT FDA UDI
Description
Curaplex IV Start Kit w/ Tegaderm, Skin Prep, Ext Set, Flush FDA UDI

Identifiers

Catalog Number
670063-KIT FDA UDI
Primary DI / UDI-DI
00815277021579 FDA UDI
FDA Product Code
FOZ FDA UDI
POQ FDA UDI
LRS FDA UDI
GMDN Term
Peripheral intravenous catheterization support kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
880.5440 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

Yes

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral intravenous catheterization support kit

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

Similar devices

Also classified as Peripheral intravenous catheterization support kit.

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

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI dc6727d4-b310-417d-861f-98bed49fd879 34 fields · synced Jun 1, 2026