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Zyphr

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Zyphr FDA UDI
Generic Name
Cranial bur, single-use FDA UDI
Device Name
8.0mm Zyphr Round Fluted FDA UDI
Model / Reference
5230010680 FDA UDI
Description
8.0mm Zyphr Round Fluted FDA UDI

Identifiers

Catalog Number
5230-010-680 FDA UDI
Primary DI / UDI-DI
04546540537485 FDA UDI
FDA Product Code
HBE FDA UDI
GMDN Term
Cranial bur, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4310 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cranial bur, single-use

Zyphr by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ef9e5f23-ba12-4881-accd-393a9bc525a3 36 fields · synced May 30, 2026