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4cis® Pinehurst Anterior Cervical Plate System

FDA UDI

Class II (US FDA UDI)

by Alphanox Co., Ltd.

Identity

Trade Name
4CIS® PINEHURST ANTERIOR CERVICAL PLATE SYSTEM FDA UDI
Generic Name
External spinal fixation system FDA UDI
Device Name
4CIS® Pinehurst Single DTS FDA UDI
Model / Reference
5932-1112 FDA UDI
Description
4CIS® Pinehurst Single DTS FDA UDI

Identifiers

Catalog Number
5932-1112 FDA UDI
Primary DI / UDI-DI
08806373581229 FDA UDI
510(k) Number
K182489 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
External spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: External spinal fixation system

4cis® Pinehurst Anterior Cervical Plate System by Alphanox Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External spinal fixation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alphanox Co., Ltd.

Sources (1)

  • FDA UDI fafca7c6-b4bc-4829-b738-9071930e74df 35 fields · synced Jun 1, 2026