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Specboard

FDA UDI

Class II (US FDA UDI)

by Macbrud Corporation

Identity

Trade Name
Specboard FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Device Name
Device Classification Name System, X-Ray, Mammographic 510(K) Number K891090 FDA UDI
Model / Reference
444 FDA UDI
Description
Device Classification Name System, X-Ray, Mammographic 510(K) Number K891090 FDA UDI

Identifiers

Primary DI / UDI-DI
B852SPECBOARD4440 FDA UDI
FDA Product Code
IZH FDA UDI
GMDN Term
Stationary x-ray grid FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1710 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Stationary x-ray grid

Specboard by Macbrud Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary x-ray grid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Macbrud Corporation

Sources (1)

  • FDA UDI 6dbf9023-7e3c-4263-a506-be3e78293b31 33 fields · synced May 30, 2026