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Ba 1/2 Kit, We, P1801, Du, 4', Dp

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
BA 1/2 KIT,WE,P1801,DU,4',DP FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
BA 1/2 KIT,WE,P1801,DU,4',DP FDA UDI
Model / Reference
BCC-5018-C04-001 FDA UDI
Description
BA 1/2 KIT,WE,P1801,DU,4',DP FDA UDI

Identifiers

Catalog Number
3655 FDA UDI
Primary DI / UDI-DI
00840828121637 FDA UDI
FDA Product Code
IQA FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3725 FDA UDI
Commercial Distribution
Not 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

Ba 1/2 Kit, We, P1801, Du, 4', Dp by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 fb059905-f9e4-4b24-896b-6bd550384a0a 36 fields · synced Jun 8, 2026