← Back to catalogue

Dtc

FDA UDI

Class I (US FDA UDI)

by Hangzhou DTC Medical Apparatus Co., Ltd.

Identity

Trade Name
DTC FDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Device Name
Stainless steel mirror FDA UDI
Model / Reference
M305 FDA UDI
Description
Stainless steel mirror FDA UDI

Identifiers

Primary DI / UDI-DI
06973554430576 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Dental mirror, reusable

Dtc by Hangzhou DTC Medical Apparatus Co., Ltd. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e99b058d-f1d3-42e3-930b-ba3261a7a8a5 33 fields · synced May 30, 2026