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Diathermy cable, for 1120 / 1121 / 1122 / 1120-0.5 / 1120-D-0.5 and 1120-0.6 han

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Diathermy cable, for 1120 / 1121 / 1122 / 1120-0.5 / 1120-D-0.5 and 1120-0.6 han FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Model / Reference
1120.A FDA UDI

Identifiers

Catalog Number
1120.A FDA UDI
Primary DI / UDI-DI
08717872000411 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

No

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

Diathermy cable, for 1120 / 1121 / 1122 / 1120-0.5 / 1120-D-0.5 and 1120-0.6 han by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II…

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 fd2f9e66-6cbb-4519-a73e-5b39b2c9649f 34 fields · synced Jun 6, 2026