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Microlyzer

FDA UDI

Class I (US FDA UDI)

by T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik Sanayi Ve Ticaret Limited Sirketi

Identity

Trade Name
MICROLYZER FDA UDI
Generic Name
Aspiration tray, single-use FDA UDI
Device Name
Single-use Blade-Filter to be used with Microlyzer Cartridge FDA UDI
Model / Reference
BLADE-FILTER 1200 FDA UDI
Description
Single-use Blade-Filter to be used with Microlyzer Cartridge FDA UDI

Identifiers

Catalog Number
BLD1200 FDA UDI
Primary DI / UDI-DI
08681092003142 FDA UDI
FDA Product Code
OJT FDA UDI
GMDN Term
Aspiration tray, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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: Aspiration tray, single-use

Microlyzer by T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik Sanayi Ve Ticaret Limited Sirketi — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Aspiration tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik Sanayi Ve Ticaret Limited Sirketi

Sources (1)

  • FDA UDI 09489b2c-7272-417a-8eae-29c1f0f92173 34 fields · synced May 30, 2026