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Belcypher Pro

FDA UDI

Class II (US FDA UDI)

by Takara Belmont Corp.

Identity

Trade Name
BELCYPHER PRO FDA UDI
Generic Name
Stationary panoramic dental x-ray system, digital FDA UDI
Device Name
BELCYPHER-PRO 120V/60HZ FDA UDI
Model / Reference
BELCYPHER PRO FDA UDI
Description
BELCYPHER-PRO 120V/60HZ FDA UDI

Identifiers

Catalog Number
BELCYPHER PRO FDA UDI
Primary DI / UDI-DI
04560217095634 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Stationary panoramic dental x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 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 panoramic dental x-ray system, digital

Belcypher Pro by Takara Belmont Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary panoramic dental x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82527009-5b04-4dfc-aaca-4eefe517988c 36 fields · synced May 30, 2026