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Spotter Device Set

FDA UDIEUDAMED

by Forum Engineering Technologies (96) Ltd.

Identity

Trade Name
Spotter Device Set FDA UDI
Generic Name
Magnetic metal detector FDA UDI
Device Name
Spotter Device set FDA UDI
Model / Reference
SPR FDA UDI
Description
Spotter Device set FDA UDI

Identifiers

Primary DI / UDI-DI
17290114352007 FDA UDI
FDA Product Code
LNF FDA UDI
GMDN Term
Magnetic metal detector FDA UDI

Classification

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Magnetic metal detector

Spotter Device Set by Forum Engineering Technologies (96) Ltd. — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic metal detector.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 82b3c0c0-cdbc-4631-9ed5-ca185007a7ba 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026