FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000301354 · Model: 8540 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000301354
Version / Model
8540
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-09
Public Version
1
Public Version Date
2022-10-17
Public Version Status
New
Public Device Record Key
16fb103f-bc3b-4bb1-967f-7d5aacd1516b

Device Description

KIT 8540 SYNCHROMED CATH ACCSS PORT EMAN

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
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
44063 Neurosurgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00763000301354

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P860004 361

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-34 – 57 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-30 – 135 Degrees Fahrenheit