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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
Coronary artery clamp FDA UDI
Device Name
COOLEY PATENT DUCTUS CLAMP, 8", STR FDA UDI
Model / Reference
HNM-1-55-6131 FDA UDI
Description
COOLEY PATENT DUCTUS CLAMP, 8", STR FDA UDI

Identifiers

Catalog Number
HNM-1-55-6131 FDA UDI
Primary DI / UDI-DI
00842962134610 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Coronary artery clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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
MRI Safety
MR Conditional FDA UDI

Category: Coronary artery clamp

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

Similar devices

Also classified as Coronary artery clamp.

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 236945f2-d8a7-414e-a670-79cab6d9b43f 34 fields · synced May 31, 2026