← Back to catalogue

Onli

FDA UDI

Class II (US FDA UDI)

by Hollister Incorporated

Identity

Trade Name
Onli FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Ready to Use Hydrophilic Intermittent Catheter, 10 Fr 16 in/40cm, Straight FDA UDI
Model / Reference
82104-30 FDA UDI
Description
Ready to Use Hydrophilic Intermittent Catheter, 10 Fr 16 in/40cm, Straight FDA UDI

Identifiers

Primary DI / UDI-DI
00610075056248 FDA UDI
FDA Product Code
GBM FDA UDI
GMDN Term
Single-administration urethral drainage catheter 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 10 French FDA UDI
Length — 16 Inch FDA UDI

Category: Single-administration urethral drainage catheter

Onli by Hollister Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-administration urethral drainage catheter.

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 2e65e3dc-f7f3-4a9d-9db7-e138dae9a8d2 36 fields · synced Jun 9, 2026