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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
Burn kit, non-medicated FDA UDI
Device Name
BURN KIT COMPLETE, W/O WATER, incl Bag, Tape and Burn Mask/Towel/Sheet Dressings FDA UDI
Model / Reference
1777-S FDA UDI
Description
BURN KIT COMPLETE, W/O WATER, incl Bag, Tape and Burn Mask/Towel/Sheet Dressings FDA UDI

Identifiers

Catalog Number
1777-S FDA UDI
Primary DI / UDI-DI
00817617028170 FDA UDI
FDA Product Code
MCY FDA UDI
GMDN Term
Burn kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Burn kit, non-medicated

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

Similar devices

Also classified as Burn kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96e1e1e8-6f96-47a5-955e-3f93e833c7f9 34 fields · synced Jun 7, 2026