← Back to catalogue

Algovita®

FDA UDI

Class III (US FDA UDI)

by Greatbatch Ltd

Identity

Trade Name
Algovita® FDA UDI
Generic Name
Neurosurgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Trial Cable Lead Marker Kit. FDA UDI
Model / Reference
5000-USA FDA UDI
Description
Trial Cable Lead Marker Kit. FDA UDI

Identifiers

Catalog Number
5000 FDA UDI
Primary DI / UDI-DI
00821329580574 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Neurosurgical procedure kit, non-medicated, single-use 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

No

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 — 213.4 Centimeter FDA UDI
Length — 81.3 Centimeter FDA UDI

Category: Neurosurgical procedure kit, non-medicated, single-use

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

Similar devices

Also classified as Neurosurgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Greatbatch Ltd

Sources (1)

  • FDA UDI a0013eb2-e8fd-4862-bacc-058577b24380 36 fields · synced Jun 6, 2026