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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
Intraosseous infusion kit FDA UDI
Device Name
Curaplex Intraosseous (IO) Infusion Kit with Jamshidi Needle 18 Gauge FDA UDI
Model / Reference
62241518S FDA UDI
Description
Curaplex Intraosseous (IO) Infusion Kit with Jamshidi Needle 18 Gauge FDA UDI

Identifiers

Catalog Number
62241518S FDA UDI
Primary DI / UDI-DI
00815277021197 FDA UDI
FDA Product Code
OKE FDA UDI
GMDN Term
Intraosseous infusion kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5965 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

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: Intraosseous infusion kit

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

Similar devices

Also classified as Intraosseous infusion kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9ae75c50-3171-4bc6-8d19-5e1f97fee647 34 fields · synced Jun 8, 2026