Struktive for Healthcare

Hospital biomedical equipment registers normalised for Nuvolo, ServiceNow, and IBM Maximo. TJC survey prep included. FDA UDI resolution and device type classification built in.

The problem

Healthcare technology management (HTM) teams maintain equipment registers across multiple systems — CMMS, spreadsheets, and legacy databases. Vendor names appear in dozens of variants, device descriptions are inconsistent, FDA UDI numbers are missing or malformed, and device type codes are absent. This makes TJC survey preparation, EAM migration, and FDA recall tracking unnecessarily difficult.

What Struktive normalises

• OEM names: GE Healthcare, Philips, Siemens Healthineers, Medtronic, Stryker, Becton Dickinson — all variants resolved to canonical form.
• Device classification: FDA device type classification for 10,000+ device types.
• FDA UDI resolution: GS1 and HIBCC UDI parsing, GUDID cross-reference for device identification.
• Location hierarchy: Building, Floor, Department, Room parsed from free-text strings.
• Quality scoring: HTM-specific scoring factors including UDI completeness, recall status, and PM schedule coverage.

Export formats

• Nuvolo / ServiceNow import CSV
• IBM Maximo Equipment Master
• TJC Survey Audit Pack
• FDA Recall Readiness Export
• FDA Device Type Classification Report

Compliance frameworks

The Joint Commission (TJC) EC.02.04.01, FDA 21 CFR Part 820, ISO 13485, HTM 00 (NHS), NFPA 99.