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Femtosecond Spatula

FDA UDI

Class I (US FDA UDI)

by Medetz Surgical Instruments

Identity

Trade Name
Femtosecond Spatula FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
Machat LASIK Retreatment Spatula DBL-Ended, Cylindrical Spatula with Slightly Pointed tip, Angled 8mm from bend to tip, / .8mm Wide Spatula, Flat Interior Edge with Rounded front tip, Angled 1.2mm from bend to tip, Round Handle FDA UDI
Model / Reference
14-2830 FDA UDI
Description
Machat LASIK Retreatment Spatula DBL-Ended, Cylindrical Spatula with Slightly Pointed tip, Angled 8mm from bend to tip, / .8mm Wide Spatula, Flat Interior Edge with Rounded front tip, Angled 1.2mm from bend to tip, Round Handle FDA UDI

Identifiers

Primary DI / UDI-DI
G2231428300 FDA UDI
FDA Product Code
HND FDA UDI
GMDN Term
Ophthalmic surgical probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical probe, reusable

Femtosecond Spatula by Medetz Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 19f23cf6-5e14-410d-a5e2-754177c608ba 34 fields · synced May 30, 2026