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Perfit ZR

FDA UDI

Class I (US FDA UDI)

by Vatech mcis Co., Ltd

Identity

Trade Name
Perfit ZR FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Model / Reference
NU 14 BL3SM W FDA UDI

Identifiers

Primary DI / UDI-DI
08800099971845 FDA UDI
FDA Product Code
EIF FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramic

Perfit ZR by Vatech mcis Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ba1297d2-995b-4835-ac9d-986fb56a677f 32 fields · synced May 31, 2026