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Michel Wound Clips

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Michel Wound Clips FDA UDI
Generic Name
General skin wound clip FDA UDI
Device Name
Michel Wound Clips Stainless Steel (100 Per Box) FDA UDI
Model / Reference
1100-780 FDA UDI
Description
Michel Wound Clips Stainless Steel (100 Per Box) FDA UDI

Identifiers

Catalog Number
1100-780 FDA UDI
Primary DI / UDI-DI
00192896120228 FDA UDI
FDA Product Code
GDT FDA UDI
GMDN Term
General skin wound clip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4760 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

Yes

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
Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 22 Millimeter FDA UDI

Category: General skin wound clip

Michel Wound Clips by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General skin wound clip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI f643226a-0d35-42fa-96d8-1fb1a0184be4 36 fields · synced May 30, 2026