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Oto-Flex

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Oto-Flex FDA UDI
Generic Name
Laryngeal knife FDA UDI
Device Name
KNIFE 3155621 OTO-FLEX 2.3MM DIAMOND FDA UDI
Model / Reference
3155621 FDA UDI
Description
KNIFE 3155621 OTO-FLEX 2.3MM DIAMOND FDA UDI

Identifiers

Primary DI / UDI-DI
00763000035884 FDA UDI
FDA Product Code
EQJ FDA UDI
ERL FDA UDI
GMDN Term
Laryngeal knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 FDA UDI
874.4250 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.3 Millimeter FDA UDI

Category: Laryngeal knife

Oto-Flex by Medtronic Xomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngeal knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 989fbcef-8ea8-4c93-9865-2707ea536b2c 35 fields · synced May 31, 2026