FDA UDI In Commercial Distribution 🇺🇸 United States

BLUE MOUNTAIN

DI: 03663422605559 · Model: 1 · SPINEWAY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BLUE MOUNTAIN
Primary DI
03663422605559
Version / Model
1
Catalog Number
412DCCL1
Company Name
SPINEWAY
Labeler DUNS
281075270
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-02
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
dda25b80-3595-4046-80c6-e62b73bedbb3

Device Description

Caspar distractor with pins, left

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03663422605559

Customer Contacts

Phone
+33472770152

Premarket Submissions

Submission Number Supplement Number
K150036 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Left