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Guide pin 20 mm

FDA UDI

Class II (US FDA UDI)

by Cochlear Bone Anchored Solutions AB

Identity

Trade Name
Guide pin 20 mm FDA UDI
Generic Name
General external orthopaedic fixation system implantation kit, single-use FDA UDI
Device Name
Laboratory component for prior generation Vistafix FDA UDI
Model / Reference
90796 FDA UDI
Description
Laboratory component for prior generation Vistafix FDA UDI

Identifiers

Catalog Number
90796 FDA UDI
Primary DI / UDI-DI
09321502016018 FDA UDI
FDA Product Code
FZE FDA UDI
GMDN Term
General external orthopaedic fixation system implantation kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3680 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 20 Millimeter FDA UDI

Category: General external orthopaedic fixation system implantation kit, single-use

Guide pin 20 mm by Cochlear Bone Anchored Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General external orthopaedic fixation system implantation kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cochlear Bone Anchored Solutions AB

Sources (1)

  • FDA UDI 334f8ca9-e5e1-4d98-88e5-164a879980f1 37 fields · synced May 30, 2026