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Mills Oschner Plaque Remover Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MILLS OSCHNER PLAQUE REMOVER FORCEPS FDA UDI
Generic Name
Endarterectomy loop FDA UDI
Device Name
MILLS OSCHNER PLAQUE REMOVER FORCEPS FDA UDI
Model / Reference
2700-0-05 FDA UDI
Description
MILLS OSCHNER PLAQUE REMOVER FORCEPS FDA UDI

Identifiers

Catalog Number
2700-0-05 FDA UDI
Primary DI / UDI-DI
00192896087637 FDA UDI
FDA Product Code
GAI FDA UDI
GMDN Term
Endarterectomy loop 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

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

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Endarterectomy loop

Mills Oschner Plaque Remover Forceps by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endarterectomy loop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9d8a8a6-847a-4e01-a3d6-c56e38317cdf 36 fields · synced May 30, 2026