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Novo Surgical

FDA UDI

Class II (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
Titanium Bipolar Bayonet Forceps, (malis type) flat handles, 8-3/4" (22.5 cm), 0.5 mm straight tip, insulated w/ irrigation FDA UDI
Model / Reference
0801-00IG FDA UDI
Description
Titanium Bipolar Bayonet Forceps, (malis type) flat handles, 8-3/4" (22.5 cm), 0.5 mm straight tip, insulated w/ irrigation FDA UDI

Identifiers

Catalog Number
0801-00IG FDA UDI
Primary DI / UDI-DI
00842331101946 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 22.5 Centimeter FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novo Surgical, Inc.

Sources (1)

  • FDA UDI 0bb4fe73-df8d-4e9a-819b-2d1376e22e06 37 fields · synced May 31, 2026