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Precision Dental Instruments

FDA UDI

Class I (US FDA UDI)

by Precision Dental Instruments

Identity

Trade Name
Precision Dental Instruments FDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Model / Reference
PI-9-79 FDA UDI

Identifiers

Catalog Number
PI-9-79 FDA UDI
Primary DI / UDI-DI
00850000052659 FDA UDI
FDA Product Code
EAX FDA UDI
GMDN Term
Dental mirror, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental mirror, reusable

Precision Dental Instruments by Precision Dental Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mirror, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a827701-9cd4-4699-867d-78bb150aa692 33 fields · synced Jun 8, 2026