← Back to catalogue

Eli Ezer

FDA UDI

Class I (US FDA UDI)

by U.s. Ophthalmic, L.l.c.

Identity

Trade Name
Eli Ezer FDA UDI
Generic Name
Perimeter, automatic FDA UDI
Device Name
Eli Ezer Perimeter EPR-3600 FDA UDI
Model / Reference
EPR-3600 FDA UDI
Description
Eli Ezer Perimeter EPR-3600 FDA UDI

Identifiers

Primary DI / UDI-DI
00851158007546 FDA UDI
FDA Product Code
HPT FDA UDI
GMDN Term
Perimeter, automatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1605 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Perimeter, automatic

Eli Ezer by U.s. Ophthalmic, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Perimeter, automatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4ac7f9c5-bfa2-45ba-922a-e2479954dcab 33 fields · synced May 30, 2026