FDA UDI In Commercial Distribution 🇺🇸 United States

Procedure Pack

DI: 07640167750344 · Model: 9.0 LCS · SIE AG, Surgical Instrument Engineering
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Procedure Pack
Primary DI
07640167750344
Version / Model
9.0 LCS
Catalog Number
510.701.190
Company Name
SIE AG, Surgical Instrument Engineering
Labeler DUNS
482163628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
2
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
e7ce308f-fe99-4643-859c-64cee73844e7

Device Description

Procedure Pack LCS Ø 9.0mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
HNO Keratome, Ac-Powered
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
45150 Ophthalmic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 07640167750887
Primary 07640167750344

Customer Contacts

Phone
8667084490

Premarket Submissions

Submission Number Supplement Number
K053511 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 9.0 Millimeter