FDA UDI In Commercial Distribution 🇺🇸 United States

Laryngeal Umbrella Keel

DI: 00815347023366 · Model: LK-16 · HOOD, E BENSON LABORATORIES INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Laryngeal Umbrella Keel
Primary DI
00815347023366
Version / Model
LK-16
Company Name
HOOD, E BENSON LABORATORIES INC
Labeler DUNS
076603380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-21
Public Version
4
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
0c46fced-3250-4473-bb44-7494cc57557f

Device Description

E. Benson Hood Laboratories Umbrella Keel

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
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
FWN Prosthesis, Larynx (Stents And Keels)

GMDN Terms

Code Name
35404 Tracheostomy tube, non-reinforced, non-customized, single-use

Identifiers

Type ID
Primary 00815347023366

Premarket Submissions

Submission Number Supplement Number
K841348 000