FDA device listing

Sirius Pintuition Base Unit

FDA device listing 1562053423 · Batenburg Applied Technologies

Key facts

Proprietary names Sirius Pintuition Base Unit
Owner/operator Batenburg Applied Technologies
Owner/operator number 10094133
Product codes NEU, PBY
Device names NEU - Marker, Radiographic, Implantable, PBY - Temporary Tissue Marker
Device class Class II
Classification regulations (21 CFR) 878.4300
Review panels General & Plastic Surgery
Registered establishments BATENBURG APPLIED TECHNOLOGIES
Establishment registrations 3036009309
FEI numbers 3036009309
Establishment operations Contract Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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