← Back to catalogue

Utrata Capsulorrhexis Fcps

FDA UDI

Class I (US FDA UDI)

by Daud Jee Mfg. Co

Identity

Trade Name
UTRATA CAPSULORRHEXIS FCPS FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
This instrument is used to grasp, retract, or stabilize tissue. FDA UDI
Model / Reference
D50-5081 FDA UDI
Description
This instrument is used to grasp, retract, or stabilize tissue. FDA UDI

Identifiers

Catalog Number
D50-5081 FDA UDI
Primary DI / UDI-DI
G006D5050810 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Utrata Capsulorrhexis Fcps by Daud Jee Mfg. Co — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

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
Daud Jee Mfg. Co

Sources (1)

  • FDA UDI 111179ee-5c34-4845-8f4a-bf602855ef61 34 fields · synced May 29, 2026