DEVICE: Axium™ (05415067025630)

Device Identifier (DI) Information

Axium™
MN23400
In Commercial Distribution
MN23400
ST. JUDE MEDICAL, INC.
05415067025630
GS1

1
149818952 *Terms of Use
Programmer Charger Kit For use with Clinical Programmer MN10700
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Device Characteristics

MR Unsafe
No
No
No
Yes
No
No
No
No

GMDN

[?]

GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
External device battery charger An electrically-powered device designed to supply an electrical charge, via a direct/wired or wireless connection, to an external parent device (i.e., nonimplantable device) or external battery pack, to recharge it for operation.
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FDA Product Code

[?]
Product Code Product Code Name
PMP Dorsal root ganglion stimulator for pain relief
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
P150004 000
P150004 005
No CLOSE

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
Special Storage Condition, Specify: Keep dry.
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

c508ae04-62a3-4b36-958b-363a835d980a
July 06, 2018
3
March 29, 2016
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
No
Yes
No CLOSE

Customer Contact

[?]
+1(855)478-5833
customerservice@sjm.com
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