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Vitalitec Shovel Retractors

FDA UDI

Class I (US FDA UDI)

by Vitalitec International, Inc.

Identity

Trade Name
Vitalitec Shovel Retractors FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
Sterilization Tray for Cygnet Clamps FDA UDI
Model / Reference
V9095 FDA UDI
Description
Sterilization Tray for Cygnet Clamps FDA UDI

Identifiers

Primary DI / UDI-DI
00857987006255 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Device sterilization/disinfection container, reusableSurgical instrument interim-placement holder, reusable

Vitalitec Shovel Retractors by Vitalitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitalitec International, Inc.

Sources (1)

  • FDA UDI 83434285-b8f0-4c75-80cb-0813b2e08a88 34 fields · synced May 30, 2026