FDA UDI In Commercial Distribution 🇺🇸 United States

CURETTE

DI: 00888118028136 · Model: 23-280-06-04 · KLS-Martin L.P.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURETTE
Primary DI
00888118028136
Version / Model
23-280-06-04
Company Name
KLS-Martin L.P.
Labeler DUNS
826499238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-26
Public Version
4
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
478e1a23-6df9-44fd-9f83-85c16a4bc067

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
FZS CURETTE, SURGICAL, GENERAL USE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00888118028136

Customer Contacts