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Nim Flex™

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
NIM FLEX™ FDA UDI
Generic Name
Reinforced endotracheal tube, single-use FDA UDI
Device Name
ENDOTRACH TUBE 8229960 5PK EMG 6MM ROHS FDA UDI
Model / Reference
8229960 FDA UDI
Description
ENDOTRACH TUBE 8229960 5PK EMG 6MM ROHS FDA UDI

Identifiers

Primary DI / UDI-DI
20643169358786 FDA UDI
510(k) Number
K925640 FDA UDI
FDA Product Code
ETN FDA UDI
GMDN Term
Reinforced endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1820 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Reinforced endotracheal tube, single-use

Nim Flex™ by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reinforced endotracheal tube, single-use.

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 211cb299-f18b-4cef-b43b-e4cf2eb32882 35 fields · synced Jun 1, 2026