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Sontec-Love Nerve Root Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC-LOVE NERVE ROOT RETRACTOR FDA UDI
Generic Name
Nerve/vessel retractor FDA UDI
Device Name
SONTEC-LOVE NERVE ROOT RETRACTOR ANGLED TIP KNURLED ROUND HANDLE FDA UDI
Model / Reference
412-608 FDA UDI
Description
SONTEC-LOVE NERVE ROOT RETRACTOR ANGLED TIP KNURLED ROUND HANDLE FDA UDI

Identifiers

Catalog Number
412-608 FDA UDI
Primary DI / UDI-DI
00192896079069 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Nerve/vessel retractor 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

Category: Nerve/vessel retractor

Sontec-Love Nerve Root Retractor by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve/vessel retractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f3c7dd6-9e6d-4754-ac0e-9486326d4ae7 36 fields · synced Jun 8, 2026