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Fan Beam Collimator Asm Symbia

FDA UDI

Class II (US FDA UDI)

by Siemens Medical Solutions Usa, Inc.

Identity

Trade Name
Fan Beam Collimator Asm Symbia FDA UDI
Generic Name
Multi-hole nuclear medicine system collimator, low-energy FDA UDI
Model / Reference
07332062 FDA UDI

Identifiers

Catalog Number
7332062.. FDA UDI
Primary DI / UDI-DI
04056869002019 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

Fan Beam Collimator Asm Symbia 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 fed03464-3ac7-4e86-99ed-3a8ce1b1771c 36 fields · synced Jun 8, 2026