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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
Eyelid speculum, single-use FDA UDI
Device Name
Barraquer Wire Speculum, Infant, Single use, 10/Box FDA UDI
Model / Reference
SSD1 1001 FDA UDI
Description
Barraquer Wire Speculum, Infant, Single use, 10/Box FDA UDI

Identifiers

Catalog Number
SSD1 1001 FDA UDI
Primary DI / UDI-DI
00810799039118 FDA UDI
FDA Product Code
HNC FDA UDI
GMDN Term
Eyelid speculum, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Eyelid speculum, single-use

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

Similar devices

Also classified as Eyelid speculum, single-use.

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 0a4f2b02-0a8e-4b82-8b16-3e0df81205f7 36 fields · synced May 31, 2026