DEVICE: NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER (00383790001250)
Device Identifier (DI) Information
NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER
15GX1" HTC-30W-D-CAP
In Commercial Distribution
FD+152530BCR-CAP
NIPRO MEDICAL CORPORATION
15GX1" HTC-30W-D-CAP
In Commercial Distribution
FD+152530BCR-CAP
NIPRO MEDICAL CORPORATION
DULL FISTULA NEEDLE for Established Access Sites Only
15Gx1" Rotating Hub 12" Tubing
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
12741 | Haemodialysis needle |
A sterile, sharp bevel-edged, hollow tubular metal instrument used to remove and return a patient's blood during a haemodialysis procedure. Commonly known as a dialysis needle. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FIE | Needle, fistula |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
8da760c7-1928-4177-9861-5b67a67425c1
March 29, 2018
2
April 01, 2016
March 29, 2018
2
April 01, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
40383790001258 | 10 | 10383790001257 | In Commercial Distribution | Case | |
10383790001257 | 50 | 00383790001250 | In Commercial Distribution | Carton |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined