FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 10649111138522 · Model: 66-1265 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Sklar®
Primary DI
10649111138522
Version / Model
66-1265
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-22
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
1134b559-7912-4515-9c5b-5dc01ba5adb8

Device Description

WIES CHAL FCP SERR 9X12MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HNR Forceps, ophthalmic

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 10649111138522