FDA UDI In Commercial Distribution 🇺🇸 United States

Sagittae

DI: 00819837020132 · Model: 521-030-00 · SPINEEX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Sagittae
Primary DI
00819837020132
Version / Model
521-030-00
Catalog Number
521-030-00
Company Name
SPINEEX, INC.
Labeler DUNS
080723590
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-06
Public Version
3
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
9a50b450-e1d1-4716-80df-87940e5de3c0

Device Description

Slap hammer

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
No
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00819837020132

Customer Contacts

Phone
5105736165