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S Spellman High Voltage Electronics Corporation

FDA UDI

Class I (US FDA UDI)

by Spellman High Voltage Electronics(Suzhou Industrial Park) Co., Ltd

Identity

Trade Name
S Spellman High Voltage Electronics Corporation FDA UDI
Generic Name
Diagnostic x-ray system generator, stationary FDA UDI
Device Name
ZR75PN40, Without console FDA UDI
Model / Reference
ZR75PN40 FDA UDI
Description
ZR75PN40, Without console FDA UDI

Identifiers

Primary DI / UDI-DI
06975490630119 FDA UDI
FDA Product Code
IZO FDA UDI
GMDN Term
Diagnostic x-ray system generator, stationary FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1700 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

Yes

FDA UDI

Category: Diagnostic x-ray system generator, stationary

S Spellman High Voltage Electronics Corporation by Spellman High Voltage Electronics(Suzhou Industrial Park) Co., Ltd — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Diagnostic x-ray system generator, stationary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c7735e13-c2ab-4cd1-948c-f7c1dfee2628 33 fields · synced Jun 8, 2026