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Perla ®

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name
PERLA ® FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
CC PREFERRED ANGLE SCREW FDA UDI
Model / Reference
CPF-CS 04 52-S FDA UDI
Description
CC PREFERRED ANGLE SCREW FDA UDI

Identifiers

Primary DI / UDI-DI
07640178976306 FDA UDI
FDA Product Code
KWP FDA UDI
NKG FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 52 Millimeter FDA UDI
Outer Diameter — 04 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Perla ® by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI 9f19e6ff-bd2d-439f-bc33-28bd8cf2913d 34 fields · synced May 30, 2026