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Q System Arthroscope

FDA UDI

Class II (US FDA UDI)

by Orthopedic Sciences, Inc

Identity

Trade Name
Q System Arthroscope FDA UDI
Generic Name
Rigid optical arthroscope, reusable FDA UDI
Device Name
3mm 0º Non-Locking Arthroscope FDA UDI
Model / Reference
AS-300 FDA UDI
Description
3mm 0º Non-Locking Arthroscope FDA UDI

Identifiers

Catalog Number
AS-300 FDA UDI
Primary DI / UDI-DI
00813892021103 FDA UDI
510(k) Number
K133018 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Rigid optical arthroscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3 Millimeter FDA UDI

Category: Rigid optical arthroscope, reusable

Q System Arthroscope by Orthopedic Sciences, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical arthroscope, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dfcf59f3-c008-4ac6-aef1-a45dd9924241 38 fields · synced May 30, 2026