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X-Cel X-Ray Corporation

FDA UDI

Class II (US FDA UDI)

by Arquilla, Inc.

Identity

Trade Name
X-CEL X-RAY CORPORATION FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, analogue FDA UDI
Device Name
PODIATRY X-RAY MACHINE, 15mA, 50-70kV FDA UDI
Model / Reference
715B-BD FDA UDI
Description
PODIATRY X-RAY MACHINE, 15mA, 50-70kV FDA UDI

Identifiers

Primary DI / UDI-DI
B216715BBD1 FDA UDI
510(k) Number
K811230 FDA UDI
FDA Product Code
KPR FDA UDI
GMDN Term
Stationary basic diagnostic x-ray system, analogue FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

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

Yes

FDA UDI

Category: Stationary basic diagnostic x-ray system, analogue

X-Cel X-Ray Corporation by Arquilla, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, analogue.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arquilla, Inc.

Sources (1)

  • FDA UDI 23f87304-838b-4bc3-988b-d26d8f9da68d 36 fields · synced May 30, 2026