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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
Skin marking pen, reusable FDA UDI
Device Name
ACKERMAN AREOLAMARKER, 5 1/2" FDA UDI
Model / Reference
HNM-M1020 FDA UDI
Description
ACKERMAN AREOLAMARKER, 5 1/2" FDA UDI

Identifiers

Catalog Number
HNM-M1020 FDA UDI
Primary DI / UDI-DI
00842962161241 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Skin marking pen, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 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: Skin marking pen, reusable

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

Similar devices

Also classified as Skin marking pen, 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 443f0fc9-5ab3-41c6-97af-a2e1b4f6fea8 34 fields · synced May 29, 2026