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Tete Cbm / Altk 250

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 19170/250

by Moria S.A.

Identity

Trade Name
TETE CBM / ALTK 250 EUDAMED
MORIA FDA UDI
Generic Name
Microkeratome FDA UDI
Device Name
TETE CBM / ALTK 250 EUDAMED
Model / Reference
19170/250 EUDAMED
CBM / ALTK HEAD 250 FDA UDI

Identifiers

Catalog Number
19170/250 FDA UDI
Primary DI / UDI-DI
03700483608201 EUDAMEDFDA UDI
Basic UDI-DI
B-03700483608201 EUDAMED
FDA Product Code
HMY FDA UDI
EMDN Code
Z1212020599 MICROKERATOMY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Microkeratome FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4370 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Tete Cbm / Altk 250 by Moria S.A. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moria S.A.
EUDAMED SRN
FR-MF-000000336

Sources (2)

  • EUDAMED f200bf41-8bc9-413b-8638-ca4b354de37f 61 fields · synced Jun 19, 2026
  • FDA UDI c32cbe0d-9400-4c32-aaf8-24634b13499b 33 fields · synced May 30, 2026