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Hnm Medical

FDA UDI

Class II (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM MEDICAL FDA UDI
Generic Name
Suprapubic catheter introducer, reusable FDA UDI
Device Name
DOUBLE END DIAMOND, 9", DIA1.1MM FDA UDI
Model / Reference
HNM-1-10-312 FDA UDI
Description
DOUBLE END DIAMOND, 9", DIA1.1MM FDA UDI

Identifiers

Catalog Number
HNM-1-10-312 FDA UDI
Primary DI / UDI-DI
00842962109748 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Suprapubic catheter introducer, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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 II — 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 e2d42de9-86cd-4105-ab38-23578866f70c 34 fields · synced May 30, 2026