← Back to catalogue

Saber-C Rasp

FDA UDI

Class I (US FDA UDI)

by Elevation Spine

Identity

Trade Name
SABER-C RASP FDA UDI
Generic Name
Internal spinal fixation procedure kit, single-use FDA UDI
Device Name
Saber-C Rasp, 12x15x5, 6 deg. FDA UDI
Model / Reference
CI-RASP2565 FDA UDI
Description
Saber-C Rasp, 12x15x5, 6 deg. FDA UDI

Identifiers

Catalog Number
CI-RASP2565 FDA UDI
Primary DI / UDI-DI
00810017913411 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Internal spinal fixation procedure kit, single-use 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

No

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

Category: Internal spinal fixation procedure kit, single-use

Saber-C Rasp by Elevation Spine — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation procedure kit, single-use.

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
Elevation Spine

Sources (1)

  • FDA UDI bf5eb3e3-44f3-43e6-a02b-81d4934b0333 34 fields · synced Jun 6, 2026