GUDIDData
enforcement Primary ID: Z-2184-2016

Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. (UDI Z-2184-2016)

Manufactured by Stryker Neurovascular

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. - Primary ID Z-2184-2016

Device Regulatory Overview

The Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. (Model/Catalog Number: Unspecified) is a medical device manufactured by Stryker Neurovascular. This product is indexed under FDA Product Code / Category Classification MODEL Number:M0035452560; Lot Number/Expiration Date: 18426504 31-May-18 18780350 31-Jan-19 18426444 31-May-18 18532556 31-Aug-18 18794332 31-Jan-19 18830452 31-Jan-19 19036717 31-May-19 19005693 30-Apr-19 19060276 31-May-19 18939358 31-Mar-19 19056621 31-May-19 19037970 31-May-19 18971989 30-Apr-19 18906402 28-Feb-19 18953265 31-Mar-19 18897969 28-Feb-19 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 →

FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter...

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

Technical Specifications

Model Number
N/A
Device Name
Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.
Database Sync Date
2026-08-09 10:06:38

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.?

The registered manufacturer of record for Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. is Stryker Neurovascular.

What is the Primary UDI-DI identifier for Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Number:M0035452560 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-2184-2016.

What classification code is assigned to this device?

This device is registered under product classification code MODEL Number:M0035452560; Lot Number/Expiration Date: 18426504 31-May-18 18780350 31-Jan-19 18426444 31-May-18 18532556 31-Aug-18 18794332 31-Jan-19 18830452 31-Jan-19 19036717 31-May-19 19005693 30-Apr-19 19060276 31-May-19 18939358 31-Mar-19 19056621 31-May-19 19037970 31-May-19 18971989 30-Apr-19 18906402 28-Feb-19 18953265 31-Mar-19 18897969 28-Feb-19.

Programmatic Export

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

JSON API Endpoint