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Sklar Instruments

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar Instruments FDA UDI
Generic Name
Vaginal speculum, single-use FDA UDI
Device Name
ECONO STERILE PEDERSON SPEC STRL MD BX/25 FDA UDI
Model / Reference
96-2615 FDA UDI
Description
ECONO STERILE PEDERSON SPEC STRL MD BX/25 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111069345 FDA UDI
FDA Product Code
HDF FDA UDI
GMDN Term
Vaginal speculum, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Vaginal speculum, single-use

Sklar Instruments by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal speculum, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 87fc9143-9f49-4d5e-ba9c-26080e8bea25 33 fields · synced May 31, 2026