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Belly Board MRI

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Belly Board MRI FDA UDI
Generic Name
Radiological pelvis positioner FDA UDI
Device Name
(glass fiber) FDA UDI
Model / Reference
126000 FDA UDI
Description
(glass fiber) FDA UDI

Identifiers

Catalog Number
126000 FDA UDI
Primary DI / UDI-DI
00841439100790 FDA UDI
510(k) Number
K121545 FDA UDI
FDA Product Code
IYE FDA UDI
LNH FDA UDI
GMDN Term
Radiological pelvis positioner FDA UDI

Classification

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Width — 19.7 Inch FDA UDI
Length — 46.5 Inch FDA UDI

Category: Radiological pelvis positioner

Belly Board MRI by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological pelvis positioner.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI ef9ee1c2-ca0b-4319-b8c9-08e7666dabb7 37 fields · synced Jun 1, 2026