Identity
- Trade Name
- Algovita® FDA UDI
- Generic Name
- Active implantable device control magnet FDA UDI
- Device Name
- Patient Magnet Kit FDA UDI
- Model / Reference
- 4900-USA FDA UDI
- Description
- Patient Magnet Kit FDA UDI
Identifiers
- Catalog Number
- 4900 FDA UDI
- Primary DI / UDI-DI
- 00821329580376 FDA UDI
- FDA Product Code
- LGW FDA UDI
- GMDN Term
- Active implantable device control magnet FDA UDI
Classification
- Device Class
- Class III 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Active implantable device control magnet
Algovita® by Greatbatch Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Active implantable device control magnet.
- VITARIA™ Patient Essentials, Model 7220 — LivaNova USA, Inc. · Class I
- Magnet — Neuropace, Inc. · Class III
- Senza — Nevro Corporation · Class III
- BIOTRONIK — BIOTRONIK SE & Co. KG · Class III
- ReActiv8 Magnet — MAINSTAY MEDICAL LIMITED · Class III
- Cyberonics® Patient Magnet — LivaNova USA, Inc. · Class I
- Axium™ — ST. JUDE MEDICAL, INC. · Class III
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Greatbatch Ltd
Sources (1)
- FDA UDI 4b5513fc-2485-4c77-b698-b700c1652be9 35 fields · synced Jun 8, 2026