FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 40649111113636 · Model: 21-764 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

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Basic Information

Brand Name
Sklar®
Primary DI
40649111113636
Version / Model
21-764
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-12-14
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
80aa5320-ea33-4d0d-be84-0a7c2b9b11ed

Device Description

BISHOP-HARMON EYE FCP 1X2 BX12

Device Characteristics

Single Use
Yes
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
No

Product Codes

Code Name
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

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

Identifiers

Type ID
Primary 40649111113636
Unit of Use 00649111113638