FDA UDI Not in Commercial Distribution 🇺🇸 United States

ProMax™ Series Bard® C-Max™ Cutting Loop

DI: 00801741018558 · Model: 355311 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
ProMax™ Series Bard® C-Max™ Cutting Loop
Primary DI
00801741018558
Version / Model
355311
Catalog Number
355311
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-23
Public Version
5
Public Version Date
2025-12-22
Public Version Status
Update
Public Device Record Key
44c776b7-48c0-4214-aa67-01a36f529bd7
Distribution End Date
2023-09-30

Device Description

ProMax™ Series Bard® C-Max™ Cutting Loop, Resectoscope Compatibility: ACMI USA Series 26 Fr.

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FAS ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Package 10801741018555
Primary 00801741018558

Customer Contacts