← Back to catalogue

Babcock Grasping Forcep Insert

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BABCOCK GRASPING FORCEP INSERT FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
BABCOCK GRASPING FORCEPS WITH CROSS-WISE TEETH DOUBLE-ACTION JAW FOR TUBE SHAFT FDA UDI
Model / Reference
2901-266 FDA UDI
Description
BABCOCK GRASPING FORCEPS WITH CROSS-WISE TEETH DOUBLE-ACTION JAW FOR TUBE SHAFT FDA UDI

Identifiers

Primary DI / UDI-DI
B09929012660 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 — 360 Millimeter FDA UDI

Babcock 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

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

Manufacturer

Sources (1)

  • FDA UDI 29747cd8-b8be-4949-b57c-3408a6b01b95 37 fields · synced Jun 6, 2026