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Piermattei Smillie Meniscotome

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
PIERMATTEI SMILLIE MENISCOTOME FDA UDI
Generic Name
Meniscus knife FDA UDI
Device Name
PIERMATTEI SMILLIE MENISCOTOME FDA UDI
Model / Reference
1103-205 FDA UDI
Description
PIERMATTEI SMILLIE MENISCOTOME FDA UDI

Identifiers

Catalog Number
1103-205 FDA UDI
Primary DI / UDI-DI
00192896052260 FDA UDI
FDA Product Code
HTS FDA UDI
GMDN Term
Meniscus knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 6.75 Inch FDA UDI

Category: Meniscus knife

Piermattei Smillie Meniscotome by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meniscus knife.

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 4f355e0e-94ec-4433-bc6e-c6dbd16a7dad 36 fields · synced Jun 8, 2026