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Maestro

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Maestro FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
PD Series Perforator Chuck FDA UDI
Model / Reference
5400210060 FDA UDI
Description
PD Series Perforator Chuck FDA UDI

Identifiers

Catalog Number
5400-210-060 FDA UDI
Primary DI / UDI-DI
04546540469229 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Surgical drill chuck FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical drill chuck

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

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 1e2482c9-883a-46c4-b3da-d6f9d506b1f5 36 fields · synced Jun 8, 2026