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Dlw, 3ld, Snap, Intellivue, "xx", Aha

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
DLW,3LD, SNAP,INTELLIVUE,"XX",AHA FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
DLW,3LD, SNAP,INTELLIVUE,"XX",AHA FDA UDI
Model / Reference
DLW-03AK-40AS-0000 FDA UDI
Description
DLW,3LD, SNAP,INTELLIVUE,"XX",AHA FDA UDI

Identifiers

Catalog Number
18130 FDA UDI
Primary DI / UDI-DI
90840828100628 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic electrode, single-use

Dlw, 3ld, Snap, Intellivue, "xx", Aha by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Curbell Medical Products, Inc.

Sources (1)

  • FDA UDI d7d18786-50aa-4519-a1ef-b8c0a0a0411b 35 fields · synced May 30, 2026