← Back to catalogue

HNM Medical

FDA UDI

Class I (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM Medical FDA UDI
Generic Name
Ear speculum, reusable FDA UDI
Device Name
FARRIOR SPECULUM, #1, 5MM, REGULAR END, RND FDA UDI
Model / Reference
HNM-1-61-0910 FDA UDI
Description
FARRIOR SPECULUM, #1, 5MM, REGULAR END, RND FDA UDI

Identifiers

Catalog Number
HNM-1-61-0910 FDA UDI
Primary DI / UDI-DI
00842962145951 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Ear speculum, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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: Ear speculum, reusable

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

Similar devices

Also classified as Ear speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hnm Stainless, Llc.

Sources (1)

  • FDA UDI 68b6b2a3-025e-47b1-a54f-8da270a76557 34 fields · synced May 29, 2026