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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
Periosteal elevator, reusable FDA UDI
Device Name
PIERCE ELEVATOR, 8 1/2", DOUBLE ENDED FDA UDI
Model / Reference
HNM-1-66-5455 FDA UDI
Description
PIERCE ELEVATOR, 8 1/2", DOUBLE ENDED FDA UDI

Identifiers

Catalog Number
HNM-1-66-5455 FDA UDI
Primary DI / UDI-DI
00842962149744 FDA UDI
FDA Product Code
KAD FDA UDI
GMDN Term
Periosteal elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Periosteal elevator, reusable

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

Similar devices

Also classified as Periosteal elevator, 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 167af5c7-950b-471f-a0ef-dcc0e41c78ca 34 fields · synced Jun 6, 2026