FDA UDI Not in Commercial Distribution 🇺🇸 United States

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DI: 10653405043584 · Model: 1-6048 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
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Primary DI
10653405043584
Version / Model
1-6048
Catalog Number
1-6048
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8931a53c-9f77-499d-b927-032b04c1030d
Distribution End Date
2017-10-10

Device Description

SELECT ONE LAPAROSCOPIC KIT

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FDE laparoscopy kit

GMDN Terms

Code Name
44096 Laparoscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10653405043584

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Bladed/Shielded Trocar
Device Size Text, specify Bladed/Shielded Surgical Trocar
Device Size Text, specify Blunt Tip Trocar
Device Size Text, specify Universal Converter
Device Size Text, specify Sleeve
Device Size Text, specify Pneumoperitoneum Insufflation Needle

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit