← Back to catalogue

S-Vector Magnet Replacement Kit

FDA UDI

Class III (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name
S-Vector Magnet Replacement Kit FDA UDI
Generic Name
ENT surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Single-Use Surgical Tool Kit FDA UDI
Model / Reference
38234 FDA UDI
Description
Single-Use Surgical Tool Kit FDA UDI

Identifiers

Primary DI / UDI-DI
09008737382346 FDA UDI
PMA Number
P000025 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
ENT surgical 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: ENT surgical procedure kit, non-medicated, single-use

S-Vector Magnet Replacement Kit by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class III — FDA UDI — listed in FDA GUDID

Similar devices

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

Cleared under the same submission

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

Sources (1)

  • FDA UDI f702870a-bc15-4f82-a442-edf3805a9d41 36 fields · synced May 30, 2026