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Innovasis® Cranial System

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Innovasis® Cranial System FDA UDI
Generic Name
Utility forceps, reusable FDA UDI
Model / Reference
LS-269 FDA UDI

Identifiers

Catalog Number
LS-269 FDA UDI
Primary DI / UDI-DI
M711LS2690 FDA UDI
FDA Product Code
GWO FDA UDI
GXR FDA UDI
HBW FDA UDI
GMDN Term
Utility forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5320 FDA UDI
882.5250 FDA UDI
882.5360 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Utility forceps, reusable

Innovasis® Cranial System by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Utility forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI 4eecbcdd-d178-4abc-a3b8-c0f3b5ec79d5 34 fields · synced May 30, 2026