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Grasping Forceps

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Grasping Forceps FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
Atraumatic Grasping Forceps With Wavy Teeth and Reservoir Double Action Jaw 5 Millimeter Diameter Shaft FDA UDI
Model / Reference
2901-245L FDA UDI
Description
Atraumatic Grasping Forceps With Wavy Teeth and Reservoir Double Action Jaw 5 Millimeter Diameter Shaft FDA UDI

Identifiers

Catalog Number
2901-245L FDA UDI
Primary DI / UDI-DI
00192896116184 FDA UDI
510(k) Number
K102921 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, reusable 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

No

FDA UDI

Dimensions & Sizes

Size
Shaft Length — 450 Millimeter FDA UDI

Category: Endoscopic electrosurgical electrode, monopolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, reusable.

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 d5f47255-1f20-4486-8ed1-cf7a35aae31a 37 fields · synced Jun 6, 2026