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Femoral Head Disarticulator Knife

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
FEMORAL HEAD DISARTICULATOR KNIFE FDA UDI
Generic Name
Meniscus knife FDA UDI
Device Name
FEMORAL HEAD DISARTICULATOR KNIFE SMALL SIZE CURVED BLADE FDA UDI
Model / Reference
1103-211 FDA UDI
Description
FEMORAL HEAD DISARTICULATOR KNIFE SMALL SIZE CURVED BLADE FDA UDI

Identifiers

Catalog Number
1103-211 FDA UDI
Primary DI / UDI-DI
00192896090040 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 — 5.5 Inch FDA UDI

Category: Meniscus knife

Femoral Head Disarticulator Knife 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 a172b5c2-dfe8-42be-a34a-003f48d924cf 36 fields · synced May 30, 2026