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Stephens Instruments

FDA UDI

Class I (US FDA UDI)

by Krishna Imports Inc

Identity

Trade Name
Stephens Instruments FDA UDI
Generic Name
Lens spoon FDA UDI
Device Name
Bunge Evisceration Spoon, Large FDA UDI
Model / Reference
S4-1210 FDA UDI
Description
Bunge Evisceration Spoon, Large FDA UDI

Identifiers

Catalog Number
S4-1210 FDA UDI
Primary DI / UDI-DI
00810799032188 FDA UDI
FDA Product Code
HNZ FDA UDI
GMDN Term
Lens spoon 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

No

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: Lens spoon

Stephens Instruments by Krishna Imports Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lens spoon.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Krishna Imports Inc

Sources (1)

  • FDA UDI 7b8bf21d-0dcd-4508-821a-f87741082d94 36 fields · synced May 30, 2026