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ASSISTO® Arm-System

FDA UDI

Class II (US FDA UDI)

by Geomed Medizin-Technik GmbH & Co. KG

Identity

Trade Name
ASSISTO® Arm-System FDA UDI
Generic Name
Surgical instrument assist arm system, manually-adjusted FDA UDI
Device Name
ASSISTO R310MM U-STAND 400X400X170MM WITH UNIVERSAL RETRACTOR HOLDER FDA UDI
Model / Reference
CA 301-20-01 FDA UDI
Description
ASSISTO R310MM U-STAND 400X400X170MM WITH UNIVERSAL RETRACTOR HOLDER FDA UDI

Identifiers

Catalog Number
CA 301-20-01 FDA UDI
Primary DI / UDI-DI
14049679076735 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Surgical instrument assist arm system, manually-adjusted FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1480 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

No

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

Category: Surgical instrument assist arm system, manually-adjusted

ASSISTO® Arm-System by Geomed Medizin-Technik GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument assist arm system, manually-adjusted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95e58613-b0ee-45fc-9031-1790b9a8e68e 34 fields · synced Jun 8, 2026