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Codman

FDA UDI

Class II (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
Codman FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
Disposable Spetzler™-Malis® Dual Irrigating Bipolar Forceps, Bayonet, 8" (20cm), 1.5mm Tip, Insulated, Non-Stick FDA UDI
Model / Reference
80-7605 FDA UDI
Description
Disposable Spetzler™-Malis® Dual Irrigating Bipolar Forceps, Bayonet, 8" (20cm), 1.5mm Tip, Insulated, Non-Stick FDA UDI

Identifiers

Catalog Number
80-7605 FDA UDI
Primary DI / UDI-DI
20886704072437 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Codman by Synergetics Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, bipolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synergetics Usa, Inc.

Sources (1)

  • FDA UDI 031a3205-de83-40a7-99e4-db6bbe66779a 35 fields · synced Jun 1, 2026