FDA UDI In Commercial Distribution 🇺🇸 United States

JULIET ® LL

DI: 07640450865540 · Model: SPE-US 00 85-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JULIET ® LL
Primary DI
07640450865540
Version / Model
SPE-US 00 85-N
Catalog Number
SPE-US 00 85-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-14
Public Version
1
Public Version Date
2022-10-24
Public Version Status
New
Public Device Record Key
10815cd5-2655-49a1-bca3-7f6ac8f85b9a

Device Description

LATERAL RASP TRIAL 21MM H08

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
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
HWT Template

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 07640450865540

Device Sizes

Type Value Unit Text
Length 21 Millimeter
Height 08 Millimeter