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SurgiMac

FDA UDI

Class I (US FDA UDI)

by Surgimac LLC

Identity

Trade Name
SurgiMac FDA UDI
Generic Name
Dental surgical probe, reusable FDA UDI
Device Name
Endo Explorer Double End 8MM Handle FDA UDI
Model / Reference
12-811-H FDA UDI
Description
Endo Explorer Double End 8MM Handle FDA UDI

Identifiers

Catalog Number
12-811-H FDA UDI
Primary DI / UDI-DI
D105SKU12811H0 FDA UDI
FDA Product Code
EMN FDA UDI
GMDN Term
Dental surgical probe, reusable 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental surgical probe, reusable

SurgiMac by Surgimac LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgimac LLC

Sources (1)

  • FDA UDI 459a903a-b81c-465b-91ec-aa05f7e33e87 34 fields · synced Jun 1, 2026