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Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, silicone FDA UDI
Device Name
PROTECTA -GEL SKIN BARRIER, FACIAL, SMALL FDA UDI
Model / Reference
301-T1126-SM FDA UDI
Description
PROTECTA -GEL SKIN BARRIER, FACIAL, SMALL FDA UDI

Identifiers

Catalog Number
301-T1126-SM FDA UDI
Primary DI / UDI-DI
00810071635755 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, silicone FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 12 Millimeter FDA UDI

Category: Dressing-fixation skin adhesive tape, silicone

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

Similar devices

Also classified as Dressing-fixation skin adhesive tape, silicone.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bb0cb699-3b1c-49d1-b263-b7c146c0c34d 35 fields · synced May 30, 2026