DEVICE: NIPRO SAFETOUCH™ II SAFETY FISTULA NEEDLE (00383790000239)
Device Identifier (DI) Information
NIPRO SAFETOUCH™ II
SAFETY FISTULA NEEDLE
17Gx1" HTC-30R/TC-30B TWIN PACK
In Commercial Distribution
FS+172530TPR
NIPRO MEDICAL CORPORATION
17Gx1" HTC-30R/TC-30B TWIN PACK
In Commercial Distribution
FS+172530TPR
NIPRO MEDICAL CORPORATION
17Gx1" Rotating Hub 11" 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.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
5eaee55c-cbb9-4aba-a96a-ac56bcb8bcda
December 20, 2018
3
April 20, 2016
December 20, 2018
3
April 20, 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 |
---|---|---|---|---|---|
40383790000237 | 10 | 10383790000236 | In Commercial Distribution | Case | |
10383790000236 | 25 | 00383790000239 | In Commercial Distribution | Carton |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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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