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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
Portable stretcher FDA UDI
Device Name
Latch Cover for Curaplex Scoop Stretcher FDA UDI
Model / Reference
14781-LC FDA UDI
Description
Latch Cover for Curaplex Scoop Stretcher FDA UDI

Identifiers

Catalog Number
14781-LC FDA UDI
Primary DI / UDI-DI
00810094576271 FDA UDI
FDA Product Code
FPP FDA UDI
GMDN Term
Portable stretcher FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable stretcher

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

Similar devices

Also classified as Portable stretcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI a10f5a52-44c5-4f86-b64e-6538f8cd1070 35 fields · synced May 30, 2026