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Malleus Nipper Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MALLEUS NIPPER FORCEPS FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
MALLEUS NIPPER UP-CUTTING FORCEPS QUANTUM FDA UDI
Model / Reference
469-110Q FDA UDI
Description
MALLEUS NIPPER UP-CUTTING FORCEPS QUANTUM FDA UDI

Identifiers

Catalog Number
469-110Q FDA UDI
Primary DI / UDI-DI
00192896093461 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 3 Inch FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

Malleus Nipper 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 ef377158-c693-4da7-8eec-8d172aa31c73 36 fields · synced May 30, 2026