SYSTEM STATUS: FDA ACTIVE ISO 13485 Valid MDR Ready
Establishment SinoTitanium
Metals
FEI No. 3033849259
Status Valid
[ISO 13485:2016 VERIFIED] // VDS- PROTOCOL ACTIVE
GDPR Compliant Protocol Active
VDS-LEGAL-2025 // DOCUMENT ID: VT-LEGAL-PRIV-2025

Privacy Policy

Data handling protocols for Valid Industrial Systems Ltd. Aligned with GDPR (EU Regulation 2016/679), CCPA, and HIPAA Business Associate requirements for medical device supply chains.

Effective Date 2025-01-01
Jurisdiction EU+US
Framework GDPR + CCPA
01

Data Controller Identity

[Entity Identification Protocol]

Legal Entity: Valid Industrial Systems Ltd (Hong Kong Company Registry: 3012XXX)

Business Purpose: Medical Device Material Supply (Class I/IIa Titanium Components)

Data Protection Officer: compliance@validti.com

EU Representative: Appointed per GDPR Article 27 (Contact via above email)

Transparency Notice: ValidTi operates as a brand. Manufacturing is executed by SinoTi (Xi'an). Data processing occurs solely within ValidTi systems. SinoTi has no independent access to customer data.

02

Data Collection Scope

[Information Capture Matrix]

A. Business Contact Data

  • Contact Info: Name, Email, Phone, Company, Job Title
  • Technical Data: Device IDs, Browser Type, IP Address (Anonymized)
  • Transaction Records: Order History, Lot Queries, Certificate Downloads

B. Data We Do NOT Collect

  • Patient Information (PHI/PII) - Not Required for B2B Supply
  • End-User Data - We Serve Dental Labs, Not Patients
  • Credit Card Data - All Payments via Bank Transfer (SWIFT)
03

Legal Basis for Processing

[GDPR Article 6 Compliance]

Processing Activity Legal Basis GDPR Article
Order Fulfillment Contractual Necessity Art. 6(1)(b)
Regulatory Traceability Legal Obligation (MDR) Art. 6(1)(c)
Marketing Communications Legitimate Interest Art. 6(1)(f)
04

Data Retention & Deletion

[Lifecycle Management Protocol]

Retention Period: 10 years from last transaction (Aligned with EU MDR Annex I, Section 18.1 - Technical Documentation Archive Requirements)

Deletion Request: Submit via compliance@validti.com. Response within 30 days per GDPR Article 17.

Limitation Notice: Records tied to active MDR post-market surveillance obligations cannot be deleted until regulatory retention periods expire (21 CFR 820.180 / EU MDR Article 10.8).

05

Third-Party Data Processors

[Subprocessor Registry]

  • Email Service: Google Workspace (GDPR-compliant Data Processing Addendum active)
  • Cloud Storage: AWS (Frankfurt Region - eu-central-1). Data residency confirmed within EU.
  • Analytics: None. We do not use Google Analytics or third-party tracking.
06

Your Rights (GDPR Chapter III)

[Data Subject Control Protocol]

✓ Right to Access

Request a copy of all data we hold about you (Art. 15)

✓ Right to Rectification

Correct inaccurate information (Art. 16)

✓ Right to Erasure

Request deletion (subject to legal retention) (Art. 17)

✓ Right to Data Portability

Receive data in machine-readable format (Art. 20)

Exercise Your Rights: Email compliance@validti.com with subject line "GDPR Request - [Your Company Name]". Identity verification required.

07

Updates & Contact

[Document Change Log]

Last Updated: 2025-01-01

Change Notification: Material changes will be announced via email to registered contacts 30 days prior to implementation.

Supervisory Authority: EU users may lodge complaints with their national Data Protection Authority. Find Your DPA

[ DATA PROTECTION CONTACT ]
Email: compliance@validti.com
Response Time: < 48 hours (Business Days)
Encryption: PGP Key Available Upon Request

Questions About Data Handling?

Contact our Data Protection Team for clarifications

Contact Compliance Team

Response Time: < 48 Hours