neoprobe

FDA UDI

Class I (US FDA UDI)

by Devicor Medical Products, Inc.

Identity

Trade Name: neoprobe FDA UDI
Generic Name: Hand-held-detector nuclear medicine system FDA UDI
Device Name: Bluetooth Straight Probe, Model 1104-CE FDA UDI
Model / Reference: NPB09S FDA UDI
Description: Bluetooth Straight Probe, Model 1104-CE FDA UDI

Identifiers

Catalog Number: CA000539001 FDA UDI
Primary DI / UDI-DI: 00841911102557 FDA UDI
FDA Product Code: IZD FDA UDI
GMDN Term: Hand-held-detector nuclear medicine system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 892.1320 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Hand-held-detector nuclear medicine system

neoprobe by Devicor Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Devicor Medical Products, Inc.

Sources (1)

FDA UDI 45ccb5ba-d7b3-4cf5-b922-14e8f8d4560c 34 fields · synced Jun 8, 2026