FDA UDI In Commercial Distribution 🇺🇸 United States

SPIDER SCREW

DI: 08057013140812 · Model: SXL-1909 · H.D.C. SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPIDER SCREW
Primary DI
08057013140812
Version / Model
SXL-1909
Catalog Number
SXL-1909
Company Name
H.D.C. SRL
Labeler DUNS
339583417
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-24
Public Version
4
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
37918f2e-4ebf-49cb-8230-a942f3eaa3ab

Device Description

SPIDER SELF- LIGATING K2 Ø 1,9x9

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OAT Implant, Endosseous, Orthodontic

GMDN Terms

Code Name
46536 Orthodontic anchoring screw

Identifiers

Type ID
Primary 08057013140812

Premarket Submissions

Submission Number Supplement Number
K091390 000