Mayfield®

FDA UDI

Class I (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name: MAYFIELD® FDA UDI
Generic Name: Medical table clamp FDA UDI
Device Name: POOL - MAYFIELD 2 Series Base Unit, Narrow FDA UDI
Model / Reference: A3100P FDA UDI
Description: POOL - MAYFIELD 2 Series Base Unit, Narrow FDA UDI

Identifiers

Catalog Number: A3100P FDA UDI
Primary DI / UDI-DI: 10381780479550 FDA UDI
FDA Product Code: FWZ FDA UDI
GMDN Term: Medical table clamp FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4950 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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Medical table clamp

Mayfield® by Integra Lifesciences Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Radial clamp — Reison Medical AB · Class I
Secure-Release — STERIS CORPORATION · Class I
COUPLER II RADIOLUCENT DORO ADAPTER, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I

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: Integra Lifesciences Corp.

Sources (1)

FDA UDI 41f7b041-0522-46f0-ae0f-4c909f505293 35 fields · synced Jun 6, 2026