FDA UDI In Commercial Distribution 🇺🇸 United States

CANNULATED PEDIGUARD

DI: 03662674000129 · Model: CANNULATED PEDIGUARD NEEDLE TROCAR 120mm · SPINEGUARD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANNULATED PEDIGUARD
Primary DI
03662674000129
Version / Model
CANNULATED PEDIGUARD NEEDLE TROCAR 120mm
Catalog Number
P2ND1101
Company Name
SPINEGUARD
Labeler DUNS
260589566
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-29
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
97e02db1-e52a-4d9f-a59c-966ed11c966b

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
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
ETN Stimulator, Nerve
PDQ Neurosurgical Nerve Locator

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Primary 03662674000129

Customer Contacts

Phone
+33145184519

Premarket Submissions

Submission Number Supplement Number
K143159 000

Device Sizes

Type Value Unit Text
Length 120 Millimeter
Outer Diameter 3.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-5 – 30 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
– 90 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
– 90 Percent (%) Relative Humidity