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Micro Neuro Biopsy Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICRO NEURO BIOPSY FORCEPS FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
MICRO NEURO BIOPSY FORCEPS LIGHTWEIGHT GOLFBALL BAYONET HANDLE STRAIGHT 360° ROTATABLE SHAFT SQUEEZE HANDLE FDA UDI
Model / Reference
2900-006 FDA UDI
Description
MICRO NEURO BIOPSY FORCEPS LIGHTWEIGHT GOLFBALL BAYONET HANDLE STRAIGHT 360° ROTATABLE SHAFT SQUEEZE HANDLE FDA UDI

Identifiers

Primary DI / UDI-DI
B09929000060 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 137fdf58-b57f-43d6-ae9f-86638a8e17a8 36 fields · synced Jun 8, 2026