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Disposable Overflow Protection / Virus Filter

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Disposable Overflow Protection / Virus Filter FDA UDI
Generic Name
Suction system filter, microbial FDA UDI
Device Name
Disposable Overflow Protection / Virus Filter, conical connection FDA UDI
Model / Reference
101035264 FDA UDI
Description
Disposable Overflow Protection / Virus Filter, conical connection FDA UDI

Identifiers

Primary DI / UDI-DI
07612367064682 FDA UDI
510(k) Number
K130123 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Suction system filter, microbial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction system filter, microbial

Disposable Overflow Protection / Virus Filter by Medela LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction system filter, microbial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medela LLC

Sources (1)

  • FDA UDI 8c8998a7-e403-47dc-8f46-a80e8024a8d8 35 fields · synced May 30, 2026