GUDIDData
enforcement Primary ID: Z-0877-2025

8MM,COBRA GRASPER,IS4000 REF 471190 (UDI Z-0877-2025)

Manufactured by Intuitive Surgical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 8MM,COBRA GRASPER,IS4000 REF 471190 - Primary ID Z-0877-2025

Device Regulatory Overview

The 8MM,COBRA GRASPER,IS4000 REF 471190 (Model/Catalog Number: Unspecified) is a medical device manufactured by Intuitive Surgical, Inc.. This product is indexed under FDA Product Code / Category Classification Model Number: 471190 Part Number: 471190-04 UDI-DI code: 00886874121481 Batch Numbers: K10230226 K10230405 K10230413 K10230420 K10231005 K10231019 K10231130 K10240104 K10240111 K10240118 K10240327 K10240418 K10240502 K10240606 K10240725 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-2753-2026 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2755-2026 View Full Alert →

FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2793-2026 View Full Alert →

SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($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 8MM,COBRA GRASPER,IS4000 REF 471190?

The registered manufacturer of record for 8MM,COBRA GRASPER,IS4000 REF 471190 is Intuitive Surgical, Inc..

What is the Primary UDI-DI identifier for 8MM,COBRA GRASPER,IS4000 REF 471190?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-0877-2025.

What classification code is assigned to this device?

This device is registered under product classification code Model Number: 471190 Part Number: 471190-04 UDI-DI code: 00886874121481 Batch Numbers: K10230226 K10230405 K10230413 K10230420 K10231005 K10231019 K10231130 K10240104 K10240111 K10240118 K10240327 K10240418 K10240502 K10240606 K10240725.

Other Devices by Intuitive Surgical, Inc.

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