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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
Non-woven gauze pad FDA UDI
Device Name
*Custom* Medic Glucose Start Kit 1EA/50EA/BX FDA UDI
Model / Reference
8600-01182 FDA UDI
Description
*Custom* Medic Glucose Start Kit 1EA/50EA/BX FDA UDI

Identifiers

Catalog Number
8600-01182 FDA UDI
Primary DI / UDI-DI
00817617020426 FDA UDI
FDA Product Code
CFW FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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: Blood lancet, single-useAdhesive bandageNon-woven gauze padAntiseptic skin towelette

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

Similar devices

Also classified as Antiseptic skin towelette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI 8d0ce139-2fda-418d-8e59-3297471377a4 34 fields · synced May 30, 2026