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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Phacoemulsification system handpiece tip, reprocessed FDA UDI
Device Name
8065751178 TURBOSONIC MINI-FLARED ABS FDA UDI
Model / Reference
065751178R FDA UDI
Description
8065751178 TURBOSONIC MINI-FLARED ABS FDA UDI

Identifiers

Catalog Number
065751178R FDA UDI
Primary DI / UDI-DI
10888277368958 FDA UDI
FDA Product Code
NKX FDA UDI
GMDN Term
Phacoemulsification system handpiece tip, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Phacoemulsification system handpiece tip, reprocessed

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification system handpiece tip, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI dbbab1c2-3a9b-4c50-9888-10fcd99d515b 35 fields · synced Jun 1, 2026