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Q-3500 Eclipse Ti-130

FDA UDI

Class I (US FDA UDI)

by Quality Aspirators, Inc.

Identity

Trade Name
Q-3500 Eclipse Ti-130 FDA UDI
Generic Name
Surgical binoculars, reusable FDA UDI
Device Name
Q-3500 Eclipse Ti-130 FDA UDI
Model / Reference
Q-3500 Eclipse Ti-130 FDA UDI
Description
Q-3500 Eclipse Ti-130 FDA UDI

Identifiers

Catalog Number
308-10030 FDA UDI
Primary DI / UDI-DI
00814005024905 FDA UDI
FDA Product Code
HJH FDA UDI
GMDN Term
Surgical binoculars, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5120 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
MRI Safety
MR Unsafe FDA UDI

Category: Surgical binoculars, reusable

Q-3500 Eclipse Ti-130 by Quality Aspirators, Inc. — 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

Sources (1)

  • FDA UDI 5167d20e-bf6c-432d-9319-40a0af373450 34 fields · synced Jun 6, 2026