← Back to catalogue

Fluid Retention Ring

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Fluid Retention Ring FDA UDI
Generic Name
Ophthalmic surgery fluid retention ring FDA UDI
Device Name
VIDAURRI FLUID RETENTION WELL 8.7MM FDA UDI
Model / Reference
K20-2135 FDA UDI
Description
VIDAURRI FLUID RETENTION WELL 8.7MM FDA UDI

Identifiers

Catalog Number
K20-2135 FDA UDI
Primary DI / UDI-DI
00841668112854 FDA UDI
FDA Product Code
HNH FDA UDI
GMDN Term
Ophthalmic surgery fluid retention ring FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Ophthalmic surgery fluid retention ring

Fluid Retention Ring by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgery fluid retention ring.

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
Katena Products, Inc.

Sources (1)

  • FDA UDI 19cccf78-1d76-4823-9535-38bc50c6094a 35 fields · synced Jun 12, 2026