← Back to catalogue

Novo Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical Inc. FDA UDI
Generic Name
Surgical fluid/gas irrigator FDA UDI
Device Name
knolle-pearce irrigating lens loop, irrigating ports at 12, 10 & 2 o'clock, 23-gauge, 1 1/4" (3.0 cm) FDA UDI
Model / Reference
OP7123-66 FDA UDI
Description
knolle-pearce irrigating lens loop, irrigating ports at 12, 10 & 2 o'clock, 23-gauge, 1 1/4" (3.0 cm) FDA UDI

Identifiers

Catalog Number
OP7123-66 FDA UDI
Primary DI / UDI-DI
00842331181795 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Surgical fluid/gas irrigator 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical fluid/gas irrigator

Novo Surgical Inc. by Novo Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical fluid/gas irrigator.

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
Novo Surgical, Inc.

Sources (1)

  • FDA UDI 7ee42ca2-4980-418e-b9eb-2b5b66a6bd07 35 fields · synced May 30, 2026