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Silicone Thoracic Catheters

FDA UDI

Class I (US FDA UDI)

by Atrium Medical Corp.

Identity

Trade Name
Silicone Thoracic Catheters FDA UDI
Generic Name
Pleural catheter FDA UDI
Device Name
7mm Mediastinal – Silicone Catheter FDA UDI
Model / Reference
14607 FDA UDI
Description
7mm Mediastinal – Silicone Catheter FDA UDI

Identifiers

Catalog Number
14607 FDA UDI
Primary DI / UDI-DI
20650862146077 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Pleural catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
Not 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

Dimensions & Sizes

Size
Outer Diameter — 7 Millimeter FDA UDI

Silicone Thoracic Catheters by Atrium Medical Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4eafab89-ac69-437d-a909-07a6f6135d62 37 fields · synced Jun 1, 2026