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SurgiTel

FDA UDI

Class I (US FDA UDI)

by Surgitel

Identity

Trade Name
SurgiTel FDA UDI
Generic Name
Surgical binoculars, reusable FDA UDI
Device Name
Optical assembly for magnified view and more ergonomic posture for surgical and dental procedures. FDA UDI
Model / Reference
MICRO300 TTL FDA UDI
Description
Optical assembly for magnified view and more ergonomic posture for surgical and dental procedures. FDA UDI

Identifiers

Primary DI / UDI-DI
00810114910085 FDA UDI
FDA Product Code
HOH FDA UDI
GMDN Term
Surgical binoculars, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4770 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: Surgical binoculars, reusable

SurgiTel by Surgitel — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical binoculars, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgitel

Sources (1)

  • FDA UDI ebdd37f3-968c-4639-b9be-bb2f20fcc215 33 fields · synced May 30, 2026