808 P37, Ig, Be, 2l

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name: 808 P37,IG,BE,2L FDA UDI
Generic Name: Electrical mains power extension cable FDA UDI
Device Name: 808 P37,IG,BE,2L FDA UDI
Model / Reference: BIC-2150-E01-8 FDA UDI
Description: 808 P37,IG,BE,2L FDA UDI

Identifiers

Catalog Number: 3920 FDA UDI
Primary DI / UDI-DI: 00840828123891 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

FDA UDI

Single Use

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

Yes

FDA UDI

Category: Electrical mains power extension cable

808 P37, Ig, Be, 2l by Curbell Medical Products, 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: Curbell Medical Products, Inc.

Sources (1)

FDA UDI 96e724db-d8ba-416b-9d32-1d5d5c65a0bc 35 fields · synced May 29, 2026