FDA UDI In Commercial Distribution 🇺🇸 United States

ProcedureKitCRF

DI: 00811746032985 · Model: CRF-U1005S-K · CAMBRIDGE INTERVENTIONAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProcedureKitCRF
Primary DI
00811746032985
Version / Model
CRF-U1005S-K
Catalog Number
CRF-U1005S-K
Company Name
CAMBRIDGE INTERVENTIONAL LLC
Labeler DUNS
080897872
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-06
Public Version
1
Public Version Date
2022-07-14
Public Version Status
New
Public Device Record Key
f021ba20-eb30-46d4-b696-5c25d9c12cd8

Device Description

CRF Procedure Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
61933 Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

Identifiers

Type ID
Primary 00811746032985

Customer Contacts

Phone
781-221-5300

Premarket Submissions

Submission Number Supplement Number
K192715 000