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Symmetry Olsen

FDA UDI

Class II (US FDA UDI)

by Olsen Medical

Identity

Trade Name
Symmetry Olsen FDA UDI
Generic Name
Electrosurgical handpiece/electrode holder, single-use FDA UDI
Model / Reference
75538 FDA UDI

Identifiers

Catalog Number
75538 FDA UDI
Primary DI / UDI-DI
00841785108969 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece/electrode holder, 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, monopolar, single-useElectrosurgical handpiece/electrode holder, single-use

Symmetry Olsen by Olsen Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece/electrode holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olsen Medical

Sources (1)

  • FDA UDI d7a1115a-b5ea-47c7-851e-c139fb48cbef 33 fields · synced May 30, 2026