FDA UDI In Commercial Distribution 🇺🇸 United States

Carnegie Surgical LLC

DI: G14150621020 · Model: 506-2102 · Carnegie Surgical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Carnegie Surgical LLC
Primary DI
G14150621020
Version / Model
506-2102
Catalog Number
506-2102
Company Name
Carnegie Surgical LLC
Labeler DUNS
017636482
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-02
Public Version
1
Public Version Date
2024-09-10
Public Version Status
New
Public Device Record Key
8f88e37a-cca6-48ac-9687-24351df2d264

Device Description

LEMPERT suction tube 8“ (20 cm) with finger cutoff and stylet 2 mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCB Tube, Tonsil Suction

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Primary G14150621020

Customer Contacts