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Epsilon USA

FDA UDI

Class I (US FDA UDI)

by Epsilon Eye Care Private Limited

Identity

Trade Name
Epsilon USA FDA UDI
Generic Name
Corneal marker, reusable FDA UDI
Device Name
Miller Rotatable Axis Marker (119 mm overall) Titanium FDA UDI
Model / Reference
ET-04 FDA UDI
Description
Miller Rotatable Axis Marker (119 mm overall) Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
G346ET040 FDA UDI
FDA Product Code
HMR FDA UDI
GMDN Term
Corneal marker, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4570 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Corneal marker, reusable

Epsilon USA by Epsilon Eye Care Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal marker, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 427e38b5-08f5-408e-994c-a2d8de95685c 34 fields · synced May 30, 2026