← 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
Skin marking pen, reusable FDA UDI
Device Name
GROSSMANN AREOLAMARKER 4 Sizes in 140,44,48,52MM FDA UDI
Model / Reference
HNM-M1000 FDA UDI
Description
GROSSMANN AREOLAMARKER 4 Sizes in 140,44,48,52MM FDA UDI

Identifiers

Catalog Number
HNM-M1000 FDA UDI
Primary DI / UDI-DI
00842962161180 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

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

Manufacturer

Manufacturer
Hnm Stainless, Llc.

Sources (1)

  • FDA UDI ac904bcc-4ef3-4d28-a7d5-e4a986d0ab31 34 fields · synced Jun 8, 2026