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Medium Energy Collimator

FDA UDI

Class II (US FDA UDI)

by Siemens Medical Solutions Usa, Inc.

Identity

Trade Name
Medium Energy Collimator FDA UDI
Generic Name
Multi-hole nuclear medicine system collimator, low-energy FDA UDI
Model / Reference
05232868 FDA UDI

Identifiers

Catalog Number
5232868.. FDA UDI
Primary DI / UDI-DI
04056869001968 FDA UDI
510(k) Number
K142006 FDA UDI
FDA Product Code
KPS FDA UDI
GMDN Term
Multi-hole nuclear medicine system collimator, low-energy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1200 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

No

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

Category: Multi-hole nuclear medicine system collimator, low-energy

Medium Energy Collimator by Siemens Medical Solutions Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-hole nuclear medicine system collimator, low-energy.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d7c9fbd-8094-4ea3-8395-6d474f88ba33 36 fields · synced Jun 8, 2026