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Sutter Medical Technologies USA, Inc

FDA UDI

Class II (US FDA UDI)

by Sutter Medical Technologies USA Inc.

Identity

Trade Name
Sutter Medical Technologies USA, Inc FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
Disposable Bipolar Forceps Cable with Flying Leads FDA UDI
Model / Reference
SUT-CF786 FDA UDI
Description
Disposable Bipolar Forceps Cable with Flying Leads FDA UDI

Identifiers

Primary DI / UDI-DI
00850006695164 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrical-only medical device connection cable, 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

Yes

FDA UDI

Category: Electrical-only medical device connection cable, single-use

Sutter Medical Technologies USA, Inc by Sutter Medical Technologies USA Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c72b0a7-27bf-483d-81a1-86e34db3d592 34 fields · synced Jun 8, 2026