← Back to catalogue

Lab Scanner

FDA UDI

Class I (US FDA UDI)

by 3shape A/S

Identity

Trade Name
Lab Scanner FDA UDI
Generic Name
Dental milling system, CAD/CAM, laboratory FDA UDI
Device Name
3Shape Articulator FDA UDI
Model / Reference
A22 FDA UDI
Description
3Shape Articulator FDA UDI

Identifiers

Primary DI / UDI-DI
05902729750608 FDA UDI
FDA Product Code
EJP FDA UDI
GMDN Term
Dental milling system, CAD/CAM, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3150 FDA UDI
Commercial Distribution
Not 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

Lab Scanner by 3shape A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
3shape A/S

Sources (1)

  • FDA UDI 67035171-4a72-400e-bbdc-8b2f726aead6 35 fields · synced Jun 7, 2026