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Algovita®

FDA UDI

Class III (US FDA UDI)

by Greatbatch Ltd

Identity

Trade Name
Algovita® FDA UDI
Generic Name
Neural-tissue electrical stimulation lead adaptor FDA UDI
Device Name
Lead Extension 8-Filar (1 X 8) FDA UDI
Model / Reference
5208-20-USA FDA UDI
Description
Lead Extension 8-Filar (1 X 8) FDA UDI

Identifiers

Catalog Number
5208-20 FDA UDI
Primary DI / UDI-DI
00821329580499 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Neural-tissue electrical stimulation lead adaptor FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI

Category: Neural-tissue electrical stimulation lead adaptor

Algovita® by Greatbatch Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neural-tissue electrical stimulation lead adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Greatbatch Ltd

Sources (1)

  • FDA UDI 509c1c28-8fca-4178-b1f3-1311f44a77e6 36 fields · synced Jun 7, 2026