VertePort

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: VertePort FDA UDI
Generic Name: Vertebral body cement cannula FDA UDI
Device Name: Cement Cannula FDA UDI
Model / Reference: 0306511000 FDA UDI
Description: Cement Cannula FDA UDI

Identifiers

Catalog Number: 0306511000 FDA UDI
Primary DI / UDI-DI: 07613252594307 FDA UDI
FDA Product Code: OAR FDA UDI
GMDN Term: Vertebral body cement cannula FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 11.0 Gauge FDA UDI

Category: Vertebral body cement cannula

VertePort by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI b1809f16-4f3b-4cd3-9b68-0971ae0771df 36 fields · synced Jun 8, 2026