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Hnm Medical

FDA UDI

Class I (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM MEDICAL FDA UDI
Generic Name
Suprapubic catheter introducer, reusable FDA UDI
Device Name
STOPCOCK LUER LOCK, 1 MALE, 2 FEMALE FDA UDI
Model / Reference
HNM-1-09-7965 FDA UDI
Description
STOPCOCK LUER LOCK, 1 MALE, 2 FEMALE FDA UDI

Identifiers

Catalog Number
HNM-1-09-7965 FDA UDI
Primary DI / UDI-DI
00842962109113 FDA UDI
FDA Product Code
FBM FDA UDI
GMDN Term
Suprapubic catheter introducer, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5090 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suprapubic catheter introducer, reusable

Hnm Medical by Hnm Stainless, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suprapubic catheter introducer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hnm Stainless, Llc.

Sources (1)

  • FDA UDI 004090e4-1695-4ef2-9e38-077d2f181edb 34 fields · synced May 30, 2026