FDA UDI In Commercial Distribution 🇺🇸 United States

Streamline OCT

DI: 00840311238880 · Model: 26-OCPGUIDE-10-12 · Surgalign Spine Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Streamline OCT
Primary DI
00840311238880
Version / Model
26-OCPGUIDE-10-12
Company Name
Surgalign Spine Technologies, Inc.
Labeler DUNS
014520584
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-05
Public Version
1
Public Version Date
2023-10-13
Public Version Status
New
Public Device Record Key
e81a4a59-4fe9-4cc5-a72c-c79b4bc2a72d

Device Description

OCP Guide, 10-12mm

Device Characteristics

Single Use
Yes
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
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00840311238880

Customer Contacts