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Assi

FDA UDI

Class I (US FDA UDI)

by Accurate Surgical & Scientific Instruments Corp.

Identity

Trade Name
ASSI FDA UDI
Generic Name
Eye spud/needle FDA UDI
Device Name
Wills Eye Hospital Foreign Body Spud And Burr Delicate Cvd. Spud End & Small Burr For Rust Ring Removal FDA UDI
Model / Reference
ASSI.16463 FDA UDI
Description
Wills Eye Hospital Foreign Body Spud And Burr Delicate Cvd. Spud End & Small Burr For Rust Ring Removal FDA UDI

Identifiers

Primary DI / UDI-DI
00841645119739 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Eye spud/needle 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Eye spud/needle

Assi by Accurate Surgical & Scientific Instruments Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye spud/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accurate Surgical & Scientific Instruments Corp.

Sources (1)

  • FDA UDI 2a5eba83-c43a-4392-8933-b82e7c5c2643 33 fields · synced May 30, 2026