← Back to catalogue

Midmark

FDA UDI

Class I (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark FDA UDI
Generic Name
Limb/torso/head restraint, reusable FDA UDI
Device Name
The Midmark Security Belt is intended to secure patients to the table during examinations and procedures. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI
Model / Reference
9A406001 FDA UDI
Description
The Midmark Security Belt is intended to secure patients to the table during examinations and procedures. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI

Identifiers

Catalog Number
9A406001 FDA UDI
Primary DI / UDI-DI
00841709111105 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Limb/torso/head restraint, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Limb/torso/head restraint, reusable

Midmark by Midmark Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb/torso/head restraint, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 31805f7e-9364-4e2e-b3f6-3dde67e413b6 35 fields · synced Jun 8, 2026