← Back to catalogue

Biolign Rotoloc

FDA UDI

Class II (US FDA UDI)

by Elite Surgical Supplies (pty) Ltd

Identity

Trade Name
Biolign Rotoloc FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Rotoloc Cervical Plate 34mm LV2 FDA UDI
Model / Reference
RL200342 FDA UDI
Description
Rotoloc Cervical Plate 34mm LV2 FDA UDI

Identifiers

Catalog Number
RL200342 FDA UDI
Primary DI / UDI-DI
06009708424556 FDA UDI
510(k) Number
K200523 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 34 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Biolign Rotoloc by Elite Surgical Supplies (pty) Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 0e7444f1-8cb7-42a1-ac00-d7c9c5da0bca 36 fields · synced Jun 1, 2026