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Dolphin Grasping Forcep Insert

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
DOLPHIN GRASPING FORCEP INSERT FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
DOLPHIN GRASPING FORCEPS WITH RESERVOIR DOUBLE-ACTION JAWS FOR TUBE SHAFT FDA UDI
Model / Reference
2901-226S FDA UDI
Description
DOLPHIN GRASPING FORCEPS WITH RESERVOIR DOUBLE-ACTION JAWS FOR TUBE SHAFT FDA UDI

Identifiers

Primary DI / UDI-DI
B0992901226S0 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, 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 — 330 Millimeter FDA UDI

Dolphin Grasping Forcep Insert 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 a5c85ded-4415-4606-9748-5bb7f50af79c 37 fields · synced May 31, 2026