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AMSure®HG Hydrophilic Intermittent Urethral Catheter

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref HG971610SS

by Amsino International, Inc.

Identity

Trade Name
AMSure® HG Hydrophilic Intermittent Urethral Catheter with water sachet and sleeve EUDAMED
AMSure®HG Hydrophilic Intermittent Urethral Catheter FDA UDI
Generic Name
Intermittent urethral drainage catheter, non-antimicrobial, single-use FDA UDI
Device Name
Hydrophilic Intermittent Catheter EUDAMED
AMSure ® HG Hydrophilic Intermittent Urethral Catheter with water sachet and sleeve 10Fr FDA UDI
Model / Reference
HG971610SS EUDAMED
1 FDA UDI
Description
AMSure ® HG Hydrophilic Intermittent Urethral Catheter with water sachet and sleeve 10Fr FDA UDI

Identifiers

Catalog Number
HG971610SS FDA UDI
Primary DI / UDI-DI
10704411008866 EUDAMEDFDA UDI
Basic UDI-DI
B-10704411008866 EUDAMED
FDA Product Code
EZD FDA UDI
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED
GMDN Term
Intermittent urethral drainage catheter, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Market of Registration
Netherlands 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

No

FDA UDI

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

AMSure®HG Hydrophilic Intermittent Urethral Catheter by Amsino International, Inc. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 403deab1-5471-4180-8991-87057ea2dd39 34 fields · synced Oct 8, 2026
  • EUDAMED e4c3b294-4b9e-42e6-9387-1300d21c4bfc 61 fields · synced Jun 19, 2026