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Pigtail Neurological Hook Probe

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
PIGTAIL NEUROLOGICAL HOOK PROBE FDA UDI
Generic Name
Bone hook FDA UDI
Device Name
PIGTAIL NEUROLOGICAL HOOK PROBE WITH LEFT SPIRAL BALL TIP FDA UDI
Model / Reference
412-444L FDA UDI
Description
PIGTAIL NEUROLOGICAL HOOK PROBE WITH LEFT SPIRAL BALL TIP FDA UDI

Identifiers

Catalog Number
412-444L FDA UDI
Primary DI / UDI-DI
00192896035485 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Bone hook 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 — 6.875 Inch FDA UDI

Category: Bone hook

Pigtail Neurological Hook Probe by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone hook.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9ca40f9-8b4c-4d0c-bdaa-803a7d2b103e 36 fields · synced Jun 6, 2026