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Lok-Bar™

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Lok-Bar™ FDA UDI
Generic Name
Radiological whole-body positioner FDA UDI
Device Name
Lok-Bar™ (2-Pin) FDA UDI
Model / Reference
MTSBRT055 FDA UDI
Description
Lok-Bar™ (2-Pin) FDA UDI

Identifiers

Catalog Number
MTSBRT055 FDA UDI
Primary DI / UDI-DI
00841439107492 FDA UDI
510(k) Number
K111340 FDA UDI
K973842 FDA UDI
FDA Product Code
IXQ FDA UDI
LNH FDA UDI
IYE FDA UDI
GMDN Term
Radiological whole-body positioner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
892.1000 FDA UDI
892.5050 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

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

Category: Radiological whole-body positioner

Lok-Bar™ by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological whole-body positioner.

Cleared under the same submission

K111340 also covers:

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 513936fd-2423-4de1-bd2c-51d4fa27745b 36 fields · synced Jun 6, 2026