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Gibeck

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
GIBECK FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Softech Bi-Flo Cannula FDA UDI
Model / Reference
IPN924726 FDA UDI
Description
Softech Bi-Flo Cannula FDA UDI

Identifiers

Catalog Number
RHET45U FDA UDI
Primary DI / UDI-DI
14026704744494 FDA UDI
510(k) Number
K961150 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Gibeck by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bd8ea34-3b7d-4ba0-ae26-3bfce75e1ebe 36 fields · synced Jun 8, 2026