← Back to catalogue

Curaplex

FDA UDI

Class II (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Electrode conductive skin pad, single-use FDA UDI
Device Name
Curaplex Select Multi-Function Defib Pads, Physio-Control Adult 10pr/cs FDA UDI
Model / Reference
16384 FDA UDI
Description
Curaplex Select Multi-Function Defib Pads, Physio-Control Adult 10pr/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00815277023931 FDA UDI
510(k) Number
K080421 FDA UDI
FDA Product Code
MLN FDA UDI
GMDN Term
Electrode conductive skin pad, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrode conductive skin pad, single-use

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

Similar devices

Also classified as Electrode conductive skin pad, single-use.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 77fa7d62-8ef0-45e5-9fc2-7b7f033bbf5d 34 fields · synced May 30, 2026