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Curaplex

FDA UDI

Class U (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Antiseptic skin towelette FDA UDI
Device Name
Curaplex Alcohol Prep Pads, Large FDA UDI
Model / Reference
1330-86100 FDA UDI
Description
Curaplex Alcohol Prep Pads, Large FDA UDI

Identifiers

Catalog Number
1330-86100 FDA UDI
Primary DI / UDI-DI
00817617027906 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Antiseptic skin towelette FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Over-the-Counter

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Antiseptic skin towelette

Curaplex by Bound Tree Medical, Llc — Class U — 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 8170afd7-1950-4590-9871-64634f499693 34 fields · synced May 30, 2026