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Multipeg

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
MULTIPEG FDA UDI
Generic Name
Dental implant stability resonance frequency analysis peg FDA UDI
Device Name
MULTIPEG FOR PENGUIN RFA FOR 4.0/5.0MM ERI FDA UDI
Model / Reference
MULTIPEG FOR PENGUIN RFA FOR 4.0/5.0MM ERI FDA UDI
Description
MULTIPEG FOR PENGUIN RFA FOR 4.0/5.0MM ERI FDA UDI

Identifiers

Catalog Number
MULTIPEG ERI 4.0/5.0 FDA UDI
Primary DI / UDI-DI
D785MULTIPEGERI40500 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental implant stability resonance frequency analysis peg FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant stability resonance frequency analysis peg

Multipeg by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant stability resonance frequency analysis peg.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI adfa149f-b70e-4bc6-88f5-ddc989efc3d4 34 fields · synced May 30, 2026