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Hnm Medical

FDA UDI

Class II (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM MEDICAL FDA UDI
Generic Name
Surgical clip remover, reusable FDA UDI
Device Name
MICHEL SUTURE CLIP, 22MM FDA UDI
Model / Reference
HNM-1-13-8022 FDA UDI
Description
MICHEL SUTURE CLIP, 22MM FDA UDI

Identifiers

Catalog Number
HNM-1-13-8022 FDA UDI
Primary DI / UDI-DI
00842962110683 FDA UDI
FDA Product Code
HBO FDA UDI
GMDN Term
Surgical clip remover, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4150 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: Surgical clip remover, reusable

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

Similar devices

Also classified as Surgical clip remover, 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 a6f5d2d3-c9a5-41d7-ac0b-d9552b72a4b0 34 fields · synced Jun 8, 2026