← Back to catalogue

Explorer Probe

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
EXPLORER PROBE FDA UDI
Generic Name
Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI
Device Name
EXPLORER PROBE WITH MARKING, 158 MM FDA UDI
Model / Reference
EXPLORER PROBE FDA UDI
Description
EXPLORER PROBE WITH MARKING, 158 MM FDA UDI

Identifiers

Catalog Number
DEP5000 FDA UDI
Primary DI / UDI-DI
B974DEP500000 FDA UDI
FDA Product Code
EKB FDA UDI
GMDN Term
Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 158 Millimeter FDA UDI

Category: Ophthalmic soft-tissue surgical forceps probe-tip, single-use

Explorer Probe by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue surgical forceps probe-tip, single-use.

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

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI d63271f4-7a4e-495c-a48b-859f52b9a022 35 fields · synced May 31, 2026