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13Ga Tapered Cannula - Trocar Stylet

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
13Ga Tapered Cannula; Trocar Stylet; Bevel Stylet FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
VP BONE ACCESS VPT13D 13GA TROCAR/BEVEL FDA UDI
Model / Reference
VPT13D FDA UDI
Description
VP BONE ACCESS VPT13D 13GA TROCAR/BEVEL FDA UDI

Identifiers

Primary DI / UDI-DI
00763000311872 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone access cannula FDA UDI
Models / Variants
Trocar Stylet FDA UDI
Bevel Stylet 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

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

Category: Bone access cannula

13Ga Tapered Cannula - Trocar Stylet by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — 3 models — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 93afb766-f8af-4c18-9ddb-dcb43f583857 35 fields · synced May 30, 2026