SnapShot Freeze 2

FDA UDI

Class II (US FDA UDI)

by Ge Medical Systems, Inc.

Identity

Trade Name: SnapShot Freeze 2 FDA UDI
Generic Name: CT system application software FDA UDI
Device Name: SnapShot Freeze Medical Device FDA UDI
Model / Reference: 1.1 FDA UDI
Description: SnapShot Freeze Medical Device FDA UDI

Identifiers

Catalog Number: 5963072 FDA UDI
Primary DI / UDI-DI: 00195278865335 FDA UDI
510(k) Number: K183161 FDA UDI
FDA Product Code: LLZ FDA UDI
JAK FDA UDI
GMDN Term: CT system application software FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.2050 FDA UDI
892.1750 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: CT system application software

SnapShot Freeze 2 by Ge Medical Systems, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Ge Medical Systems, Inc.

Sources (1)

FDA UDI 0e09a3a8-4e98-4d31-afc8-8dea9cf42520 35 fields · synced May 30, 2026