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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
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
EMESIS BASIN, 26OZ FDA UDI
Model / Reference
HNM-1-10 FDA UDI
Description
EMESIS BASIN, 26OZ FDA UDI

Identifiers

Catalog Number
HNM-1-10 FDA UDI
Primary DI / UDI-DI
00842962109519 FDA UDI
FDA Product Code
FNY FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 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: Surgical instrument interim-placement holder, reusable

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

Similar devices

Also classified as Surgical instrument interim-placement holder, 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 e064eecf-c047-42b4-9c6b-343e2a86ce5e 34 fields · synced Jun 8, 2026