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Guide Pin

FDA UDI

Class I (US FDA UDI)

by Etgar - Medical Instruments Ltd

Identity

Trade Name
Guide Pin FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
Guide Pin 13 mm FDA UDI
Model / Reference
ET-0132 FDA UDI
Description
Guide Pin 13 mm FDA UDI

Identifiers

Primary DI / UDI-DI
07290112447388 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable 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

No

FDA UDI

Implantable

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Dental implantation depth/angle gauge, reusable

Guide Pin by Etgar - Medical Instruments Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3969c46e-a927-4d07-ac5e-91e199094da7 33 fields · synced Jun 8, 2026