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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
Pneumothorax catheter insertion set FDA UDI
Device Name
KIT DECOMPRESSION KIT FOR QUEEN ANNE'S CO FDA UDI
Model / Reference
QASEEPNEK FDA UDI
Description
KIT DECOMPRESSION KIT FOR QUEEN ANNE'S CO FDA UDI

Identifiers

Catalog Number
QASEEPNEK FDA UDI
Primary DI / UDI-DI
00812277033748 FDA UDI
FDA Product Code
FMG FDA UDI
GMDN Term
Pneumothorax catheter insertion set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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: Pneumothorax catheter insertion set

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

Similar devices

Also classified as Pneumothorax catheter insertion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de552e14-3c9a-483e-8c1b-5a27162fae17 34 fields · synced May 30, 2026