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Case Medical

FDA UDI

Class II (US FDA UDI)

by Case Medical Inc

Identity

Trade Name
CASE MEDICAL FDA UDI
Generic Name
Sterilization container filter, single-use FDA UDI
Device Name
CONTAINER FILTER NON-WOVEN 7.5" DIA. (500 PK) FDA UDI
Model / Reference
SCF02-5 FDA UDI
Description
CONTAINER FILTER NON-WOVEN 7.5" DIA. (500 PK) FDA UDI

Identifiers

Catalog Number
SCF02-5 FDA UDI
Primary DI / UDI-DI
00653159012587 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Sterilization container filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sterilization container filter, single-use

Case Medical by Case Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization container filter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Case Medical Inc

Sources (1)

  • FDA UDI e208835c-0fe7-4cd5-afd0-6147450290df 34 fields · synced Jun 8, 2026