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X-OMAT EX II Developer and Replenisher

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
X-OMAT EX II Developer and Replenisher FDA UDI
Generic Name
X-ray film processing chemical, automatic FDA UDI
Device Name
10GL X-OMAT EX II DEV RPLR FDA UDI
Model / Reference
X-OMAT EX II Developer and Replenisher FDA UDI
Description
10GL X-OMAT EX II DEV RPLR FDA UDI

Identifiers

Catalog Number
1135433 FDA UDI
Primary DI / UDI-DI
60889971135438 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
X-ray film processing chemical, automatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1840 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray film processing chemical, automaticX-ray film processing chemical, manual

X-OMAT EX II Developer and Replenisher by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film processing chemical, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fbe6ba66-7c12-4a2c-a1f8-561fff6eb3c0 34 fields · synced Jun 8, 2026