← Back to catalogue

Slim-Loc

FDA UDI

Class I (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
SLIM-LOC FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
SLIM-LOC ANTERIOR CERVICAL PLATE SYSTEM Drill for 14mm Screw FDA UDI
Model / Reference
465174 FDA UDI
Description
SLIM-LOC ANTERIOR CERVICAL PLATE SYSTEM Drill for 14mm Screw FDA UDI

Identifiers

Catalog Number
465174 FDA UDI
Primary DI / UDI-DI
10705034003191 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
Not 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Slim-Loc by Cerenovus, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cerenovus, Inc.

Sources (1)

  • FDA UDI c4b55c3c-6e1c-4b90-b5de-987645bbcc68 36 fields · synced May 30, 2026