Map-iT

FDA UDI

Class II (US FDA UDI)

by Access Point Technologies, Inc.

Identity

Trade Name: Map-iT FDA UDI
Generic Name: Electrocardiographic lead/catheter adaptor FDA UDI
Device Name: Shrouded Deca Extension Cable, Steerable 10 pole, Black, Reusable FDA UDI
Model / Reference: 901956 FDA UDI
Description: Shrouded Deca Extension Cable, Steerable 10 pole, Black, Reusable FDA UDI

Identifiers

Catalog Number: 901956 FDA UDI
Primary DI / UDI-DI: 00818087020299 FDA UDI
FDA Product Code: IKD FDA UDI
GMDN Term: Electrocardiographic lead/catheter adaptor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.1175 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Hydrogen Peroxide FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 150 Centimeter FDA UDI

Category: Electrocardiographic lead/catheter adaptor

Map-iT by Access Point Technologies, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Access Point Technologies, Inc.

Sources (1)

FDA UDI 6c3696d2-1506-4ac1-9fae-c0f804d23eea 36 fields · synced May 30, 2026