FDA UDI In Commercial Distribution 🇺🇸 United States

KLOCKNER

DI: 08435451629302 · Model: 10 06 22 P · SOADCO, S.L.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KLOCKNER
Primary DI
08435451629302
Version / Model
10 06 22 P
Catalog Number
10 06 22 P
Company Name
SOADCO, S.L.
Labeler DUNS
464517122
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-22
Public Version
1
Public Version Date
2022-11-30
Public Version Status
New
Public Device Record Key
0b8a6e3f-6536-4d77-b25b-dedb8c5ce8fb

Device Description

SURGICAL BOX KLOCKNER EXTERNAL [EMPTY]

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
45147 Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 08435451629302

Customer Contacts

Phone
+376800593

Premarket Submissions

Submission Number Supplement Number
K173642 000