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Meniscotome V-Blade

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MENISCOTOME V-BLADE FDA UDI
Generic Name
Meniscus knife FDA UDI
Device Name
MENISCOTOME V-BLADE SHAPED FLAT HANDLE FDA UDI
Model / Reference
1103-206 FDA UDI
Description
MENISCOTOME V-BLADE SHAPED FLAT HANDLE FDA UDI

Identifiers

Catalog Number
1103-206 FDA UDI
Primary DI / UDI-DI
00192896052277 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

Meniscotome V-Blade 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 2b3e7aaa-d50a-4f97-9b54-7cb4f2065e3d 36 fields · synced May 30, 2026