← Back to catalogue

Delphi CF

FDA UDI

Class I (US FDA UDI)

by Avante

Identity

Trade Name
Delphi CF FDA UDI
Generic Name
Fluoroscopy/angiography table top FDA UDI
Model / Reference
70G6000 FDA UDI

Identifiers

Primary DI / UDI-DI
00815871022415 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Fluoroscopy/angiography table top FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluoroscopy/angiography table top

Delphi CF by Avante — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluoroscopy/angiography table top.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Avante

Sources (1)

  • FDA UDI dc24348d-9863-4352-915b-681a4af2a0bc 33 fields · synced May 30, 2026