Kyphon® Multi-tap™ Adapter

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name: Kyphon® Multi-tap™ Adapter FDA UDI
Generic Name: Orthopaedic cement dispenser FDA UDI
Device Name: MULTI-TAP ADAPTER A22 SIZE 2 AAC FDA UDI
Model / Reference: A22 FDA UDI
Description: MULTI-TAP ADAPTER A22 SIZE 2 AAC FDA UDI

Identifiers

Primary DI / UDI-DI: 00643169142664 FDA UDI
FDA Product Code: KIH FDA UDI
GMDN Term: Orthopaedic cement dispenser 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

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

FDA UDI

Manufacturing Date

FDA UDI

Category: Orthopaedic cement dispenser

Kyphon® Multi-tap™ Adapter by Medtronic Sofamor Danek, Inc. — 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: Medtronic Sofamor Danek, Inc.

Sources (1)

FDA UDI adf829b5-ea8d-4ffb-a173-700de96659c2 34 fields · synced May 30, 2026