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Sutter

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 700940

by Sutter Medizintechnik GmbH

Identity

Trade Name
Sutter FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
Bipolar Clamps EUDAMED
Bipolar Clamp Calvian®, EU 15° angled, with suction, WL 12 cm FDA UDI
Model / Reference
700940 EUDAMEDFDA UDI
Description
Bipolar Clamp Calvian®, EU 15° angled, with suction, WL 12 cm FDA UDI

Identifiers

Catalog Number
700940 FDA UDI
Primary DI / UDI-DI
ESUM7009400 EUDAMEDFDA UDI
Basic UDI-DI
++ESUMTD11700900C3 EUDAMED
Direct Marketing DI
ESUM7009400 EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
L180401 OPEN ELECTROSURGERY FORCEPS, REUSABLE EUDAMED
GMDN Term
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Sutter by Sutter Medizintechnik GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 2d5fb96e-23b8-4af1-866e-c72790ee042d 34 fields · synced Jul 9, 2026
  • EUDAMED 2840a618-e220-4039-88c8-a3aef30abd36 61 fields · synced Jul 9, 2026