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Perfecto

FDA UDI

Class II (US FDA UDI)

by Crown Delta Corp.

Identity

Trade Name
PERFECTO FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
PERFECTO LIGHT BODY SHM YELLOW REGULAR SET - 50 mL CARTRIDGE FDA UDI
Model / Reference
DW62 FDA UDI
Description
PERFECTO LIGHT BODY SHM YELLOW REGULAR SET - 50 mL CARTRIDGE FDA UDI

Identifiers

Catalog Number
DW62 FDA UDI
Primary DI / UDI-DI
00818524020240 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Silicone dental impression material

Perfecto by Crown Delta Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Crown Delta Corp.

Sources (1)

  • FDA UDI c2fd3cf5-b3d9-4762-9ef5-0229b54edecb 35 fields · synced Jun 8, 2026