← Back to catalogue

Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar® FDA UDI
Generic Name
Eyelid speculum, reusable FDA UDI
Device Name
WEEKS EYE SPEC 3" 15X5MM LOOP FDA UDI
Model / Reference
65-1730 FDA UDI
Description
WEEKS EYE SPEC 3" 15X5MM LOOP FDA UDI

Identifiers

Primary DI / UDI-DI
10649111007392 FDA UDI
FDA Product Code
HNC FDA UDI
GMDN Term
Eyelid speculum, 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Eyelid speculum, reusable

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

Similar devices

Also classified as Eyelid speculum, 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
Sklar Corporation

Sources (1)

  • FDA UDI 833b91d2-151a-4080-abb9-87d87b7c7cd3 33 fields · synced May 31, 2026