← Back to catalogue

Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Pneumothorax dressing FDA UDI
Device Name
T.O.C.S. Tactical Occlusive Chest Seal - Vented FDA UDI
Model / Reference
1215-22196 FDA UDI
Description
T.O.C.S. Tactical Occlusive Chest Seal - Vented FDA UDI

Identifiers

Catalog Number
1215-22196 FDA UDI
Primary DI / UDI-DI
00812277034905 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Pneumothorax dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

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

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
Radiation Sterilization FDA UDI

Category: Pneumothorax dressing

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

Similar devices

Also classified as Pneumothorax dressing.

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 d534d464-28b0-41f3-afed-436f614f288d 34 fields · synced May 30, 2026