FDA UDI In Commercial Distribution 🇺🇸 United States

SYNCHROMED™ III

DI: 00763000999421 · Model: 8667-40 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SYNCHROMED™ III
Primary DI
00763000999421
Version / Model
8667-40
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-15
Public Version
1
Public Version Date
2026-01-23
Public Version Status
New
Public Device Record Key
e227d814-06a4-46f0-ad9f-5e9581109c39

Device Description

PUMP 8667-40 SYNCHROMEDIII EMAN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LKK Pump, infusion, implanted, programmable

GMDN Terms

Code Name
46024 Implantable intrathecal infusion pump, programmable

Identifiers

Type ID
Primary 00763000999421

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P860004 434

Device Sizes

Type Value Unit Text
Device Size Text, specify Reservoir Volume 40 mL

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from Magnets