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Hollister

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 72084

by Hollister Incorporated

Identity

Trade Name
Hollister EUDAMED
VaPro FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
No Touch Urethral Intermittent Catheter, Nelaton EUDAMED
No Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve FDA UDI
Model / Reference
72084 EUDAMEDFDA UDI
Description
No Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve FDA UDI

Identifiers

Primary DI / UDI-DI
00610075081196 EUDAMEDFDA UDI
Basic UDI-DI
610075D03P081S0258C4 EUDAMED
Unit of Use DI
00610075065387 EUDAMED
510(k) Number
K141642 FDA UDI
FDA Product Code
GBM FDA UDI
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED
GMDN Term
Single-administration urethral drainage catheter FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 8 French FDA UDI
Length — 16 Inch FDA UDI

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

Hollister by Hollister Incorporated — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000027818
Authorised Representative
Hollister ULC IE-AR-000022119

Sources (2)

  • EUDAMED c65d4a10-ed15-45a0-840f-ff327a380de9 61 fields · synced Jun 9, 2026
  • FDA UDI 779b331a-0d2d-4e42-9cea-eb54370d448c 37 fields · synced May 29, 2026