Perla ® Tl

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name: PERLA ® TL FDA UDI
Generic Name: Bone file/rasp, manual, reusable FDA UDI
Device Name: GUIDED REAMER FDA UDI
Model / Reference: TLF-IN 11 30-N FDA UDI
Description: GUIDED REAMER FDA UDI

Identifiers

Catalog Number: TLF-IN 11 30-N FDA UDI
Primary DI / UDI-DI: 07640185349872 FDA UDI
FDA Product Code: KWP FDA UDI
NKB FDA UDI
GMDN Term: Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3050 FDA UDI
888.3070 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Spineart

Sources (1)

FDA UDI a0aa3fcd-2357-4a26-81d0-208205e54c49 34 fields · synced Jun 6, 2026