← Back to catalogue

Apollo DRF

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 9784G95331

by Villa Sistemi Medicali S.p.A.

Identity

Trade Name
Apollo DRF EUDAMED
Villa Sistemi Medicali FDA UDI
Generic Name
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
Device Name
Apollo EUDAMED
Model / Reference
9784G95331 EUDAMED
Apollo DRF FDA UDI

Identifiers

Primary DI / UDI-DI
08057737120114 EUDAMEDFDA UDI
Basic UDI-DI
805773712FT2209C EUDAMED
Direct Marketing DI
08057737120114 EUDAMED
510(k) Number
K050190 FDA UDI
FDA Product Code
KXJ FDA UDI
IXL FDA UDI
KPW FDA UDI
EMDN Code
Z11030702 DIGITAL REMOTE CONTROL TABLES EUDAMED
GMDN Term
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
892.1670 FDA UDI
892.1610 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Apollo DRF by Villa Sistemi Medicali S.p.a. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IT-MF-000016860

Sources (2)

  • EUDAMED 9ab04e82-291b-4a00-8f0e-19e852953972 61 fields · synced Jul 30, 2026
  • FDA UDI acb7cee3-eeb8-422f-8d00-fa3aee2250a9 33 fields · synced May 29, 2026