← Back to catalogue

Curaplex

FDA UDI

Class II (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
Curaplex Sharps Container, 32 Quart 1EA 10EA/CS FDA UDI
Model / Reference
1860-08705 FDA UDI
Description
Curaplex Sharps Container, 32 Quart 1EA 10EA/CS FDA UDI

Identifiers

Catalog Number
1860-08705 FDA UDI
Primary DI / UDI-DI
00810071635786 FDA UDI
510(k) Number
K942054 FDA UDI
FDA Product Code
MMK FDA UDI
GMDN Term
Sharps container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sharps container

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

Similar devices

Also classified as Sharps container.

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 a925edd8-d3bb-4c27-871a-1dc56a927cfa 35 fields · synced May 30, 2026