FDA UDI In Commercial Distribution 🇺🇸 United States

Sherlock

DI: 00801741124389 · Model: 9770300 · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Sherlock
Primary DI
00801741124389
Version / Model
9770300
Catalog Number
9770300
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
cb61b997-71e4-408c-9c82-1c20d2db5986

Device Description

SHERLOCK 3CG DIAMOND UPGRADE KIT

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LJS Catheter,intravascular,therapeutic,long-term greater than 30 days

GMDN Terms

Code Name
61667 Central venous catheter navigation system, electrocardiographic/magnetic

Identifiers

Type ID
Primary 00801741124389

Customer Contacts