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Endo-diathermy handle, straight pointed tip.(23 gauge / 0.6 mm)

FDA UDI

Class II (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
Endo-diathermy handle, straight pointed tip.(23 gauge / 0.6 mm) FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Model / Reference
1120.06 FDA UDI

Identifiers

Catalog Number
1120.06 FDA UDI
Primary DI / UDI-DI
08717872000404 FDA UDI
510(k) Number
K190875 FDA UDI
FDA Product Code
HQR FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4100 FDA UDI
Commercial Distribution
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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Endo-diathermy handle, straight pointed tip.(23 gauge / 0.6 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI…

Similar devices

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

Cleared under the same submission

K190875 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5158b44b-11f8-4590-9935-8e3417c798f4 34 fields · synced Jun 8, 2026