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Vitom

FDA UDI

Class I (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
VITOM FDA UDI
Generic Name
Surgical instrument assist arm system, power-adjusted FDA UDI
Device Name
VITOM 3D clamping jaw for POINT SETTER FDA UDI
Model / Reference
28272VTP FDA UDI
Description
VITOM 3D clamping jaw for POINT SETTER FDA UDI

Identifiers

Primary DI / UDI-DI
04048551387726 FDA UDI
FDA Product Code
EPT FDA UDI
GMDN Term
Surgical instrument assist arm system, power-adjusted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 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

Yes

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, power-adjusted

Vitom by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI d67c3e72-a8c8-4e66-ac0c-dda0d0764d62 33 fields · synced May 30, 2026