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320, 103 P37, Sy, Be, 2l, 2ld, Be (p103)

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
320,103 P37,SY,BE,2L,2LD,BE (P103) FDA UDI
Generic Name
Electrical mains power extension cable FDA UDI
Device Name
320,103 P37,SY,BE,2L,2LD,BE (P103) FDA UDI
Model / Reference
IC-1460 FDA UDI
Description
320,103 P37,SY,BE,2L,2LD,BE (P103) FDA UDI

Identifiers

Catalog Number
16109 FDA UDI
Primary DI / UDI-DI
00840828127592 FDA UDI
FDA Product Code
ILQ FDA UDI
GMDN Term
Electrical mains power extension cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3710 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical mains power extension cable

320, 103 P37, Sy, Be, 2l, 2ld, Be (p103) by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical mains power extension cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c93b30f6-9d0a-40bb-8d8d-91be5517ed90 35 fields · synced May 31, 2026