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EndoWrist

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 471172

by Intuitive Surgical, Inc.

Identity

Trade Name
Maryland Bipolar Forceps EUDAMED
EndoWrist FDA UDI
Generic Name
Robotic electrosurgical instrument, bipolar, reusable FDA UDI
Device Name
Bipolar Instruments EUDAMED
MARYLAND BIPOLAR FORCEPS FDA UDI
Model / Reference
471172 EUDAMEDFDA UDI
Description
MARYLAND BIPOLAR FORCEPS FDA UDI

Identifiers

Primary DI / UDI-DI
00886874119792 EUDAMEDFDA UDI
Basic UDI-DI
0886874119969AT EUDAMED
Direct Marketing DI
00886874119792 EUDAMED
FDA Product Code
NAY FDA UDI
EMDN Code
L1304 ROBOTIC SURGERY FORCEPS AND GRASPERS, REUSABLE EUDAMED
GMDN Term
Robotic electrosurgical instrument, bipolar, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
876.1500 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

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 8 Millimeter FDA UDI

Category: Robotic electrosurgical instrument, bipolar, reusable

EndoWrist by Intuitive Surgical, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Robotic electrosurgical instrument, 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 21f4b3d7-fa1f-48ec-af41-088dd280ed6a 34 fields · synced Sep 17, 2026
  • EUDAMED 07742361-4c02-4376-b83d-6c164c86005b 61 fields · synced Sep 17, 2026