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Posterior Crown and Bridge Impression System Kit

FDA UDI

Class II (US FDA UDI)

by Moving Islands Transit Inc

Identity

Trade Name
Posterior Crown and Bridge Impression System Kit FDA UDI
Generic Name
Dental impression material kit, reusable FDA UDI
Device Name
Kit Contains: 6 x MiTi Heavy Body VPS Impression Material, 1 x MiTi Light Body VPS Impression Material, 18 x 88 mm Heavy Body Teal Mixing Tips, 18 x 70 mm Light Body Yellow Mixing Tips, 18 Intraoral Tips, 18 MiTi Posterior Mesh Bite Trays FDA UDI
Model / Reference
627843379591 FDA UDI
Description
Kit Contains: 6 x MiTi Heavy Body VPS Impression Material, 1 x MiTi Light Body VPS Impression Material, 18 x 88 mm Heavy Body Teal Mixing Tips, 18 x 70 mm Light Body Yellow Mixing Tips, 18 Intraoral Tips, 18 MiTi Posterior Mesh Bite Trays FDA UDI

Identifiers

Primary DI / UDI-DI
00627843379591 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Dental impression material kit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental impression material kit, reusable

Posterior Crown and Bridge Impression System Kit by Moving Islands Transit Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression material kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da79f592-584c-48a7-88b2-e575fd9f0f3b 35 fields · synced May 30, 2026