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Disc Filter

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Disc Filter FDA UDI
Generic Name
Medication transfer needle, filtering FDA UDI
Device Name
1.2 Micron SUPOR® Aspiration / Injection Disc Filter FDA UDI
Model / Reference
414995 FDA UDI
Description
1.2 Micron SUPOR® Aspiration / Injection Disc Filter FDA UDI

Identifiers

Catalog Number
414995 FDA UDI
Primary DI / UDI-DI
04022495769763 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Medication transfer needle, filtering FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medication transfer needle, filtering

Disc Filter by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer needle, filtering.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1402ee9c-6dec-4699-9121-a9e547e6a0ca 35 fields · synced May 31, 2026