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Runnels Steerable Introducer™ #5 Nasal

FDA UDI

Class I (US FDA UDI)

by Through The Cords, Llc

Identity

Trade Name
Runnels Steerable Introducer™ #5 Nasal FDA UDI
Generic Name
Endotracheal tube introducer, single-use FDA UDI
Device Name
Pre-lubricated articulating introducer with intuitive colored depth system, 91.5 CM, 15 Fr, latex free, single use, sterile, fits 6.0 and larger ID tubes. FDA UDI
Model / Reference
001079 FDA UDI
Description
Pre-lubricated articulating introducer with intuitive colored depth system, 91.5 CM, 15 Fr, latex free, single use, sterile, fits 6.0 and larger ID tubes. FDA UDI

Identifiers

Primary DI / UDI-DI
00850059297001 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Endotracheal tube introducer, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5790 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

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

Yes

FDA UDI

Category: Endotracheal tube introducer, single-use

Runnels Steerable Introducer™ #5 Nasal by Through The Cords, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube introducer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f81022ac-b8fc-43d5-b626-f8768f436453 34 fields · synced May 30, 2026