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Hopkins Medical Products®

FDA UDI

Class II (US FDA UDI)

by Hopkins Uniform Company

Identity

Trade Name
Hopkins Medical Products® FDA UDI
Generic Name
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI
Device Name
Foley Catheter 100% Silicone, 20Fr 30cc FDA UDI
Model / Reference
34203 FDA UDI
Description
Foley Catheter 100% Silicone, 20Fr 30cc FDA UDI

Identifiers

Catalog Number
34203 FDA UDI
Primary DI / UDI-DI
00817643020155 FDA UDI
510(k) Number
K040504 FDA UDI
FDA Product Code
EZL FDA UDI
GMDN Term
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Indwelling urethral drainage balloon catheter, non-antimicrobial

Hopkins Medical Products® by Hopkins Uniform Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indwelling urethral drainage balloon catheter, non-antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cd3cb144-6f5a-4dff-bffc-91d8c541834a 36 fields · synced May 31, 2026