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Sentimag

FDA UDI

Class II (US FDA UDI)

by Endomagnetics Ltd

Identity

Trade Name
Sentimag FDA UDI
Generic Name
Magnetic metal detector FDA UDI
Device Name
Probe checker for Sentimag Gen 3 Probe FDA UDI
Model / Reference
Gen 3 Probe Checker FDA UDI
Description
Probe checker for Sentimag Gen 3 Probe FDA UDI

Identifiers

Catalog Number
SMC03 FDA UDI
Primary DI / UDI-DI
15060391210343 FDA UDI
FDA Product Code
NEU FDA UDI
PUV FDA UDI
GMDN Term
Magnetic metal detector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Magnetic metal detector

Sentimag by Endomagnetics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic metal detector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endomagnetics Ltd

Sources (1)

  • FDA UDI 7b44a7af-5a3c-4303-a1f2-172f1779a680 34 fields · synced Jun 8, 2026