← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
TUBING AND CONNECTORS,BREAST PUMP,2PCS FDA UDI
Model / Reference
MDS68108 FDA UDI
Description
TUBING AND CONNECTORS,BREAST PUMP,2PCS FDA UDI

Identifiers

Catalog Number
MDS68108 FDA UDI
Primary DI / UDI-DI
10197344006212 FDA UDI
FDA Product Code
HGX FDA UDI
GMDN Term
Breast pump, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5160 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

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breast pump, electric

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast pump, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3004e8a6-4a71-4fe1-a71e-3e8b723de110 36 fields · synced May 30, 2026