FDA UDI In Commercial Distribution 🇺🇸 United States

CANNULATED PEDIGUARD

DI: 03662674000594 · Model: Needle XS, Trocar, 130mm · SPINEGUARD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CANNULATED PEDIGUARD
Primary DI
03662674000594
Version / Model
Needle XS, Trocar, 130mm
Catalog Number
P2ND2201
Company Name
SPINEGUARD
Labeler DUNS
260589566
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-18
Public Version
1
Public Version Date
2025-09-26
Public Version Status
New
Public Device Record Key
99c939ee-31ce-4c04-8432-88da21487bcf

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
SCY Sacroiliac Joint Guidewire Placement Device

GMDN Terms

Code Name
60478 Bone access cannula

Identifiers

Type ID
Primary 03662674000594

Customer Contacts

Phone
+33145184519

Premarket Submissions

Submission Number Supplement Number
K241895 000