FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00814716020883 · Model: HMA-1040F · COASTAL LIFE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00814716020883
Version / Model
HMA-1040F
Company Name
COASTAL LIFE TECHNOLOGIES, INC.
Labeler DUNS
809254670
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
49df1394-e034-46b2-b5a5-eb7463a6106d

Device Description

Fiber Optic Cable, Single-Use Disposable

Device Characteristics

Single Use
Yes
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
No
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
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47785 Urogenital surgical laser system beam guide, single-use

Identifiers

Type ID
Package 10814716020880
Primary 00814716020883