← Back to catalogue

Cobra®

FDA UDI

Class II (US FDA UDI)

by Neurovision Medical Products, Inc.

Identity

Trade Name
Cobra® FDA UDI
Generic Name
Electromyographic endotracheal tube FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
B006LTE7003PSD52 FDA UDI
FDA Product Code
ETN FDA UDI
BTR FDA UDI
GWF FDA UDI
GXZ FDA UDI
IKT FDA UDI
GMDN Term
Electromyographic endotracheal tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1820 FDA UDI
868.5730 FDA UDI
882.1870 FDA UDI
882.1350 FDA UDI
890.1385 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromyographic needle electrode, single-useNerve-locating system probe, single-useElectromyographic endotracheal tube

Cobra® by Neurovision Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromyographic endotracheal tube.

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

Manufacturer
Neurovision Medical Products, Inc.

Sources (1)

  • FDA UDI 741603d6-eed9-4c2b-91df-9bcbc4f7a943 32 fields · synced Jun 8, 2026