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Eyejet® Ctr

FDA UDI

Class III (US FDA UDI)

by Morcher GmbH

Identity

Trade Name
EYEJET® CTR FDA UDI
Generic Name
Capsular tension ring FDA UDI
Device Name
SINGLE-USE PRE-LOADED CAPSULAR TENSION RING FDA UDI
Model / Reference
14 RIGHT V.3 FDA UDI
Description
SINGLE-USE PRE-LOADED CAPSULAR TENSION RING FDA UDI

Identifiers

Primary DI / UDI-DI
04048509392024 FDA UDI
PMA Number
P010059 FDA UDI
FDA Product Code
MRJ FDA UDI
GMDN Term
Capsular tension ring FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capsular tension ring

Eyejet® Ctr by Morcher GmbH — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capsular tension ring.

Cleared under the same submission

P010059 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Morcher GmbH

Sources (1)

  • FDA UDI e024c165-c4c1-4ebd-a81e-a3e49b66b690 35 fields · synced May 31, 2026