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Lateral Stabilizer

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Lateral Stabilizer FDA UDI
Generic Name
Indexed-immobilization patient positioning system FDA UDI
Device Name
Reusable non-sterile lateral stabilizer for use with Siemens Somatom Sensation CT FDA UDI
Model / Reference
MTIL600311 FDA UDI
Description
Reusable non-sterile lateral stabilizer for use with Siemens Somatom Sensation CT FDA UDI

Identifiers

Catalog Number
MTIL600311 FDA UDI
Primary DI / UDI-DI
00841439105245 FDA UDI
510(k) Number
K973842 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Indexed-immobilization patient positioning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 16.8 Inch FDA UDI
Width — 9.4 Inch FDA UDI

Lateral Stabilizer by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K973842 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI 1f4b2b6b-e711-49eb-b583-3435e3f49f0e 38 fields · synced May 31, 2026