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Serial connection vacuum

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Serial connection vacuum FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Model / Reference
077.0095 FDA UDI

Identifiers

Primary DI / UDI-DI
07612367015288 FDA UDI
FDA Product Code
BTA FDA UDI
CGX FDA UDI
KDQ FDA UDI
QPB FDA UDI
GMDN Term
Surgical suction system collection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
862.1225 FDA UDI
880.6740 FDA UDI
878.5040 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: Surgical suction system collection container, reusable

Serial connection vacuum by Medela LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medela LLC

Sources (1)

  • FDA UDI b4895490-e527-4c3e-9075-99b87669d294 33 fields · synced May 31, 2026