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Directa FullForm

FDA UDI

Class I (US FDA UDI)

by Directa AB

Identity

Trade Name
Directa FullForm FDA UDI
Generic Name
Dental mould FDA UDI
Model / Reference
C I-1 FDA UDI

Identifiers

Catalog Number
609632 FDA UDI
Primary DI / UDI-DI
17310236096327 FDA UDI
FDA Product Code
ELZ FDA UDI
GMDN Term
Dental mould FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Dental mould

Directa FullForm by Directa AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mould.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Directa AB

Sources (1)

  • FDA UDI f4876ebf-edfe-4555-9126-1ae0e647ddff 33 fields · synced Jun 8, 2026