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dose-map™

FDA UDI

Class II (US FDA UDI)

by Ashland Specialty Ingredients, G.P.

Identity

Trade Name
dose-map™ FDA UDI
Generic Name
X-ray film cassette holder FDA UDI
Device Name
blood irradiator dosimetry system FDA UDI
Model / Reference
Biobeam 2000 Custom FDA UDI
Description
blood irradiator dosimetry system FDA UDI

Identifiers

Catalog Number
943965 FDA UDI
Primary DI / UDI-DI
00810106410579 FDA UDI
FDA Product Code
IXA FDA UDI
GMDN Term
X-ray film cassette holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1850 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray film cassette holder

dose-map™ by Ashland Specialty Ingredients, G.P. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59fb9fe4-001d-45d2-b962-96995fd059d0 34 fields · synced Jun 9, 2026