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Plastic Sleeve for Multi-Unit

FDA UDI

Class I (US FDA UDI)

by Etgar - Medical Instruments Ltd

Identity

Trade Name
Plastic Sleeve for Multi-Unit FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Plastic Sleeve for Multi-Unit Screw included FDA UDI
Model / Reference
EI-4988 FDA UDI
Description
Plastic Sleeve for Multi-Unit Screw included FDA UDI

Identifiers

Primary DI / UDI-DI
07290112444301 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
MRI Safety
MR Conditional FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Plastic Sleeve for Multi-Unit by Etgar - Medical Instruments Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 839ab68e-2d5a-4942-b92b-261c756f0393 33 fields · synced Jun 1, 2026