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Biopsy Cup Insert

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BIOPSY CUP INSERT FDA UDI
Generic Name
Open-surgery biopsy forceps, reusable FDA UDI
Device Name
BIOPSY CUP LONG WITH THORN SINGLE-ACTION JAWS FOR TUBE SHAFT FDA UDI
Model / Reference
2901-129 FDA UDI
Description
BIOPSY CUP LONG WITH THORN SINGLE-ACTION JAWS FOR TUBE SHAFT FDA UDI

Identifiers

Primary DI / UDI-DI
B09929011290 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery biopsy 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

Biopsy Cup 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 6b79cbe8-30bd-4583-bd66-33c1a0021b47 37 fields · synced Jun 8, 2026