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ScanBox pro - Candid

FDA UDI

Class I (US FDA UDI)

by Dental Monitoring

Identity

Trade Name
ScanBox pro - Candid FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Device Name
Phone support + Cheek retractor ScanBoxpro L Pack. The kit contains 2 elements: -1 Cheek Retractor: Large size (L). -1 Phone support. FDA UDI
Model / Reference
001 FDA UDI
Description
Phone support + Cheek retractor ScanBoxpro L Pack. The kit contains 2 elements: -1 Cheek Retractor: Large size (L). -1 Phone support. FDA UDI

Identifiers

Catalog Number
1011-001 FDA UDI
Primary DI / UDI-DI
03770021392176 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Dental cheek retractor, professional, 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

Yes

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

Category: Dental cheek retractor, professional, reusableDental cheek retractor, home-use

ScanBox pro - Candid by Dental Monitoring — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cheek retractor, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dental Monitoring

Sources (1)

  • FDA UDI 3f14db45-f28d-4f9c-bb5d-c4535c477a2d 35 fields · synced Jun 8, 2026