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Deleey Centerline Posterior With Linear Metal

FDA UDI

Class II (US FDA UDI)

by Productora Y Comercializadora Odontologica New Stetic S A

Identity

Trade Name
Deleey Centerline Posterior With Linear Metal FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Deleey Centerline Posterior Without Linear Metal FDA UDI
Model / Reference
23005 FDA UDI
Description
Deleey Centerline Posterior Without Linear Metal FDA UDI

Identifiers

Catalog Number
23005 FDA UDI
Primary DI / UDI-DI
07701126550020 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Resin artificial teeth

Deleey Centerline Posterior With Linear Metal by Productora Y Comercializadora Odontologica New Stetic S A — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5daf719-9f7f-407a-960d-ebf44b13f8b2 34 fields · synced May 31, 2026