FDA UDI In Commercial Distribution 🇺🇸 United States

Spine Pro

DI: 00848657067294 · Model: 2804 · NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spine Pro
Primary DI
00848657067294
Version / Model
2804
Company Name
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Labeler DUNS
839138955
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-26
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
dbc97ee2-fe25-4f0d-bca9-249421d00951

Device Description

Spine Pro Bayonet Kerrison, 4mm, 230mm, 40 degree

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
HAE RONGEUR, MANUAL

GMDN Terms

Code Name
35287 Bone punch, reusable

Identifiers

Type ID
Primary 00848657067294

Premarket Submissions

Submission Number Supplement Number
K023868 000