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G-Series Assistant's Binocular Observation Tube, White, 3-Axis Rotation - Requir

FDA UDI

Class I (US FDA UDI)

by Global Surgical Corp.

Identity

Trade Name
G-SERIES ASSISTANT'S BINOCULAR OBSERVATION TUBE, WHITE, 3-AXIS ROTATION - REQUIR FDA UDI
Generic Name
General-purpose surgical microscope FDA UDI
Model / Reference
M W1023C FDA UDI

Identifiers

Primary DI / UDI-DI
00810040251795 FDA UDI
FDA Product Code
EPT FDA UDI
GMDN Term
General-purpose surgical microscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical microscope

G-Series Assistant's Binocular Observation Tube, White, 3-Axis Rotation - Requir by Global Surgical Corp. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as General-purpose surgical microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2955b30e-1461-410c-820c-95c4c05d93cb 32 fields · synced Jun 6, 2026