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Bipolar Jensen Bayonet Forceps

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BIPOLAR JENSEN BAYONET FORCEPS FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
BIPOLAR JENSEN BAYONET FORCEPS FLAT HANDLE INSULATED NON STICK FDA UDI
Model / Reference
2700-890NS FDA UDI
Description
BIPOLAR JENSEN BAYONET FORCEPS FLAT HANDLE INSULATED NON STICK FDA UDI

Identifiers

Primary DI / UDI-DI
B0992700890NS0 FDA UDI
510(k) Number
K101080 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Bipolar Jensen Bayonet Forceps by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 193cc233-9f7d-49ff-a767-7e0e5e816230 37 fields · synced May 31, 2026