HMG facial Cannula 18G NS

FDA UDI

Class I (US FDA UDI)

by Hartman Medical Group, LLC

Identity

Trade Name: HMG facial Cannula 18G NS FDA UDI
Generic Name: Tissue injection cannula FDA UDI
Device Name: Cannula, Facial, 18gx80mm, Non- Sterile FDA UDI
Model / Reference: FC18G080NS FDA UDI
Description: Cannula, Facial, 18gx80mm, Non- Sterile FDA UDI

Identifiers

Primary DI / UDI-DI: 10850048235127 FDA UDI
FDA Product Code: GEA FDA UDI
GMDN Term: Tissue injection cannula FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Tissue injection cannula

HMG facial Cannula 18G NS by Hartman Medical Group, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Hartman Medical Group, LLC

Sources (1)

FDA UDI 85e88487-1c5f-4011-a2a4-c85d98341b8e 33 fields · synced Jun 8, 2026