GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: CEB01016

eyeMAX(TM) Extraction Basket (UDI CEB01016)

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 eyeMAX(TM) Extraction Basket - Primary ID CEB01016

Device Regulatory Overview

The eyeMAX(TM) Extraction Basket (Model/Catalog Number: CEB01016) is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification LQR 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
CEB01016
Product Code / EMDN
LQR
Device Name
"Basket shape: Four wires spiral; Basket Diameter: 15mm; Basket Length: 40mm;Working Length: 600mm;
Database Sync Date
2026-08-09 09:24:49

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 eyeMAX(TM) Extraction Basket?

The registered manufacturer of record for eyeMAX(TM) Extraction Basket is Micro-Tech (Nanjing) Co., Ltd..

What is the Primary UDI-DI identifier for eyeMAX(TM) Extraction Basket?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CEB01016.

What classification code is assigned to this device?

This device is registered under product classification code LQR.

Similar Classification Devices (LQR)

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

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