GUDIDData
enforcement Primary ID: Z-1932-2017

AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system (UDI Z-1932-2017)

Manufactured by The Anspach Effort, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system - Primary ID Z-1932-2017

Device Regulatory Overview

The AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system (Model/Catalog Number: Unspecified) is a medical device manufactured by The Anspach Effort, Inc.. This product is indexed under FDA Product Code / Category Classification All product shipped prior to 09/27/2016; DFU 18-0040 Part No. AL-III-DISS-30 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
AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
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 AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system?

The registered manufacturer of record for AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system is The Anspach Effort, Inc..

What is the Primary UDI-DI identifier for AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-1932-2017.

What classification code is assigned to this device?

This device is registered under product classification code All product shipped prior to 09/27/2016; DFU 18-0040 Part No. AL-III-DISS-30.

Programmatic Export

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

JSON API Endpoint