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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
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Curaplex IV Dressing, Site-Loc, Transparent, Latex Free, 2 3/8 in x 2 3/4 in, 100/bx 4bx/cs FDA UDI
Model / Reference
1830-12113 FDA UDI
Description
Curaplex IV Dressing, Site-Loc, Transparent, Latex Free, 2 3/8 in x 2 3/4 in, 100/bx 4bx/cs FDA UDI

Identifiers

Catalog Number
1830-12113 FDA UDI
Primary DI / UDI-DI
00812277037418 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

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

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 90aed838-e952-4b12-b531-e9a6e0bf88a8 34 fields · synced May 31, 2026