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Portex

FDA UDI

Class I (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
Portex FDA UDI
Generic Name
Tracheobronchial suction/insufflation catheter, single-lumen FDA UDI
Model / Reference
Z210-12 FDA UDI

Identifiers

Primary DI / UDI-DI
15019315046896 FDA UDI
FDA Product Code
BSY FDA UDI
CAF FDA UDI
GMDN Term
Tracheobronchial suction/insufflation catheter, single-lumen FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
868.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tracheobronchial suction/insufflation catheter, single-lumen

Portex by Icu Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheobronchial suction/insufflation catheter, single-lumen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI adeae916-b11a-4f1b-9202-561199bff412 32 fields · synced May 30, 2026