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Suction jar, 2 ltr

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Suction jar, 2 ltr FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
Suction jar, polysulfone, 2 l, OKM, K7503763 FDA UDI
Model / Reference
080.0024 FDA UDI
Description
Suction jar, polysulfone, 2 l, OKM, K7503763 FDA UDI

Identifiers

Primary DI / UDI-DI
07612367007023 FDA UDI
510(k) Number
K150134 FDA UDI
FDA Product Code
BTA 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
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

Suction jar, 2 ltr 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.

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 5427b20c-20c2-47bc-a1a0-0e5af26614b8 34 fields · synced Jun 1, 2026