← Back to catalogue

Codman Y-Connector, 4-prong device only, unpackaged

FDA UDI

Class II (US FDA UDI)

by Bipad, Inc.

Identity

Trade Name
Codman Y-Connector, 4-prong device only, unpackaged FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
4 pole Y connector FDA UDI
Model / Reference
BP105-CY4 FDA UDI
Description
4 pole Y connector FDA UDI

Identifiers

Catalog Number
BP105-CY4 FDA UDI
Primary DI / UDI-DI
00860003991824 FDA UDI
510(k) Number
K201833 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Codman Y-Connector, 4-prong device only, unpackaged by Bipad, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, bipolar, single-use.

Cleared under the same submission

K201833 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bipad, Inc.

Sources (1)

  • FDA UDI 955db5ec-c194-4c44-a0e3-6a2e8d52786a 35 fields · synced Jun 8, 2026