← 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
Uterine sound, reusable FDA UDI
Device Name
HEGAR DILATOR, 7 1/4", DIA 14MM FDA UDI
Model / Reference
HNM-1-52-3014 FDA UDI
Description
HEGAR DILATOR, 7 1/4", DIA 14MM FDA UDI

Identifiers

Catalog Number
HNM-1-52-3014 FDA UDI
Primary DI / UDI-DI
00842962127148 FDA UDI
FDA Product Code
GCC FDA UDI
GMDN Term
Uterine sound, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Uterine sound, reusable

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

Similar devices

Also classified as Uterine sound, 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 6ec3811d-cf5d-4b42-979b-1a3a1d333e75 34 fields · synced May 31, 2026