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NeuroPro®

FDA UDI

Class II (US FDA UDI)

by Kinamed, Inc.

Identity

Trade Name
NeuroPro® FDA UDI
Generic Name
Cranioplasty sheet FDA UDI
Device Name
Plate Panel, Heavy, 0.6mm FDA UDI
Model / Reference
14-1P3-8622 FDA UDI
Description
Plate Panel, Heavy, 0.6mm FDA UDI

Identifiers

Catalog Number
14-1P3-8622 FDA UDI
Primary DI / UDI-DI
00898142001173 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Cranioplasty sheet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Cranioplasty sheet

NeuroPro® by Kinamed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cranioplasty sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kinamed, Inc.

Sources (1)

  • FDA UDI a7f71852-342e-4e2c-a74b-2016939ccf95 34 fields · synced Jun 6, 2026