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Senhance

FDA UDI

Class II (US FDA UDI)

by Asensus Surgical, Inc.

Identity

Trade Name
Senhance FDA UDI
Generic Name
Robotic surgical arm system FDA UDI
Device Name
Adapter, Strong Grasper, Long FDA UDI
Model / Reference
X9007012 FDA UDI
Description
Adapter, Strong Grasper, Long FDA UDI

Identifiers

Catalog Number
200-21058 FDA UDI
Primary DI / UDI-DI
00815440020408 FDA UDI
510(k) Number
K171120 FDA UDI
FDA Product Code
NAY FDA UDI
GMDN Term
Robotic surgical arm system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Robotic surgical arm system

Senhance by Asensus Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Robotic surgical arm system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e36ff5f4-547d-4924-82de-fece794629bd 35 fields · synced Sep 18, 2026