FDA UDI In Commercial Distribution 🇺🇸 United States

J & J INSTRUMENTS

DI: 00817524020397 · Model: 02-275 · J & J INSTRUMENTS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
J & J INSTRUMENTS
Primary DI
00817524020397
Version / Model
02-275
Catalog Number
02-275
Company Name
J & J INSTRUMENTS INC
Labeler DUNS
783328149
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-31
Public Version
2
Public Version Date
2023-06-28
Public Version Status
Update
Public Device Record Key
85544cd5-a781-452a-a34b-daa48e27302b

Device Description

LUCAS CURETTE #75

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
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
EKE Curette, Operative

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00817524020397

Device Sizes

Type Value Unit Text
Length 7 Inch