← Back to catalogue

Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
*CUSTOM* Shelby Co Blood Draw Kit FDA UDI
Model / Reference
8600-01331 FDA UDI
Description
*CUSTOM* Shelby Co Blood Draw Kit FDA UDI

Identifiers

Catalog Number
8600-01331 FDA UDI
Primary DI / UDI-DI
00812277031959 FDA UDI
FDA Product Code
CBT FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arterial blood sampling kit

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

Similar devices

Also classified as Arterial blood sampling 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 8c549050-b95a-4f2a-9f80-e15ccad519b9 34 fields · synced Jun 8, 2026