CORE, Maestro

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: CORE, Maestro FDA UDI
Generic Name: Foot-switch, pneumatic FDA UDI
Device Name: Universal Footpedal FDA UDI
Model / Reference: 5400218000 FDA UDI
Description: Universal Footpedal FDA UDI

Identifiers

Catalog Number: 5400-218-000 FDA UDI
Primary DI / UDI-DI: 07613154410224 FDA UDI
FDA Product Code: HBB FDA UDI
GMDN Term: Foot-switch, pneumatic 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

FDA UDI

Single Use

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Foot-switch, pneumatic

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

Similar devices

Also classified as Foot-switch, pneumatic.

MicroAire® — MicroAire Surgical Instruments LLC · Class I
ELAN 4 — AESCULAP, INC. · Class II
De Soutter Medical — De Soutter Medical, Ltd. · Class I
Senhance Ultrasonic — Asensus Surgical, Inc. · Class II
MICRO 100 — Conmed Corporation · Class I
AESCULAP — AESCULAP, INC. · Class II
De Soutter Medical — De Soutter Medical, Ltd. · Class I
PlumeVac — Conmed Corporation · Class II

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 II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 4e63f33f-9683-49d6-ac31-f4fd1964a22d 36 fields · synced Jun 8, 2026