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Arthroscopic Grasping & Biopsy Rongeur Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
ARTHROSCOPIC GRASPING & BIOPSY RONGEUR FORCEPS FDA UDI
Generic Name
Open-surgery biopsy forceps, reusable FDA UDI
Device Name
GRASPING RONGUER BIOPSY FORCEPS SERRATED 3.4 MILLIMETER CUP TUBULAR SHAFT 4.0 INCHES FDA UDI
Model / Reference
1271-018 FDA UDI
Description
GRASPING RONGUER BIOPSY FORCEPS SERRATED 3.4 MILLIMETER CUP TUBULAR SHAFT 4.0 INCHES FDA UDI

Identifiers

Catalog Number
1271-018 FDA UDI
Primary DI / UDI-DI
00192896056350 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Open-surgery biopsy forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Open-surgery biopsy forceps, reusable

Arthroscopic Grasping & Biopsy Rongeur Forceps by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fe88ad9c-253b-4aa9-bf3e-8724eebb5be8 36 fields · synced Jun 8, 2026