GUDIDData
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gudid Primary ID: 00823C

Disposable Biopsy Forceps (UDI 00823C)

Manufactured by Micro-Tech (Nanjing) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Disposable Biopsy Forceps - Primary ID 00823C

Device Regulatory Overview

The Disposable Biopsy Forceps (Model/Catalog Number: 00823C) is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FCL within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0237-2019 View Full Alert →

Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1877-2018 View Full Alert →

Trident Endoscopic Ultrasonic Biopsy Needle (FNB)...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1878-2018 View Full Alert →

Trident Endoscopic Ultrasonic Aspiration Needle (FNA)...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
00823C
Product Code / EMDN
FCL
Device Name
Precisor handle,Cam structure,10FR,2300mm,Alligator forceps with needle,PE coated
Database Sync Date
2026-08-09 09:11:07

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Disposable Biopsy Forceps?

The registered manufacturer of record for Disposable Biopsy Forceps is Micro-Tech (Nanjing) Co., Ltd..

What is the Primary UDI-DI identifier for Disposable Biopsy Forceps?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00823C.

What classification code is assigned to this device?

This device is registered under product classification code FCL.

Similar Classification Devices (FCL)

Other Devices by Micro-Tech (Nanjing) Co., Ltd.

Programmatic Export

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