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800 P37, Je, Be, 2l, Std, 790

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
800 P37,JE,BE,2L,STD,790 FDA UDI
Generic Name
Electrical mains power extension cable FDA UDI
Device Name
800 P37,JE,BE,2L,STD,790 FDA UDI
Model / Reference
BIC-19C0-E05-8 FDA UDI
Description
800 P37,JE,BE,2L,STD,790 FDA UDI

Identifiers

Catalog Number
15300 FDA UDI
Primary DI / UDI-DI
00840828133890 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

800 P37, Je, Be, 2l, Std, 790 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 525e2ff1-4db8-48c0-a832-627bcc2d3922 35 fields · synced May 30, 2026