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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
Urethral dilator, reusable FDA UDI
Device Name
DISPOSABLE OS FINDER, BOX OF 25 FDA UDI
Model / Reference
HBI-OS265BA-1 FDA UDI
Description
DISPOSABLE OS FINDER, BOX OF 25 FDA UDI

Identifiers

Catalog Number
HBI-OS265BA-1 FDA UDI
Primary DI / UDI-DI
00842962106457 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Urethral dilator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
Not 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

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

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 e94b6726-570f-414e-9d83-6806ff29c6b5 35 fields · synced May 30, 2026