← Back to catalogue

ID Round Ring

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
ID Round Ring FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
ID Round Segmented Ring 8-1/2 " FDA UDI
Model / Reference
9900-18 FDA UDI
Description
ID Round Segmented Ring 8-1/2 " FDA UDI

Identifiers

Catalog Number
9900-18 FDA UDI
Primary DI / UDI-DI
10840199542229 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retractor/retraction system blade, reusable

ID Round Ring by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI a1a60617-630d-468d-ae32-6dd1fe6497a8 37 fields · synced May 31, 2026