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Arthroscopic Biopsy Grasping Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
ARTHROSCOPIC BIOPSY GRASPING FORCEPS FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
ARTHROSCOPIC BIOPSY GRASPING FORCEPS WITH/WITHOUT RATCHET OVERLOAD CONE STRAIGHT TIP FDA UDI
Model / Reference
1270-101R FDA UDI
Description
ARTHROSCOPIC BIOPSY GRASPING FORCEPS WITH/WITHOUT RATCHET OVERLOAD CONE STRAIGHT TIP FDA UDI

Identifiers

Catalog Number
1270-101R FDA UDI
Primary DI / UDI-DI
00192896083936 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Rigid endoscopic 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

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 97be2f40-2f80-4146-a0b1-6fc070b91f41 36 fields · synced May 31, 2026