FDA UDI In Commercial Distribution 🇺🇸 United States

Precisor Broncho

DI: 30653405052115 · Model: 100503 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Precisor Broncho
Primary DI
30653405052115
Version / Model
100503
Catalog Number
100503
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-11-28
Public Version
1
Public Version Date
2020-12-07
Public Version Status
New
Public Device Record Key
b340873a-bd48-47c5-831c-d17c08bbce57

Device Description

Precisor Broncho Pulmonary Costed Disposable Biopsy Forceps

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
FCL FORCEPS, BIOPSY, NON-ELECTRIC

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Package 10653405052111
Primary 30653405052115
Unit of Use 00653405052114

Customer Contacts

Device Sizes

Type Value Unit Text
Length 115 Centimeter
Depth 2 Millimeter
Width 1.8 Millimeter