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Bevel

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Bevel FDA UDI
Generic Name
Bone access channel kit FDA UDI
Device Name
NTRODUCER T34E KYPHON EX OI BEVEL FDA UDI
Model / Reference
T34E FDA UDI
Description
NTRODUCER T34E KYPHON EX OI BEVEL FDA UDI

Identifiers

Primary DI / UDI-DI
00763000311759 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone access channel kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone access channel kit

Bevel by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access channel kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 496e6626-2e0e-4426-a132-6385ebc7d652 35 fields · synced Jun 8, 2026