← Back to catalogue

Perla ®

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name
PERLA ® FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Screwdriver T20 FDA UDI
Model / Reference
CPF-IN 13 02-N FDA UDI
Description
Screwdriver T20 FDA UDI

Identifiers

Catalog Number
CPF-IN 13 02-N FDA UDI
Primary DI / UDI-DI
07640178981768 FDA UDI
FDA Product Code
KWP FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 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

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

Category: Surgical screwdriver, reusable

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

Similar devices

Also classified as Surgical screwdriver, reusable.

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
Spineart

Sources (1)

  • FDA UDI dd2f8838-9aef-4cc5-8f91-3b1e8c4f4a6b 34 fields · synced May 31, 2026