FDA UDI In Commercial Distribution 🇺🇸 United States

Procedure Pack

DI: 07640167750146 · Model: 8.5/110 · SIE AG, Surgical Instrument Engineering
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Procedure Pack
Primary DI
07640167750146
Version / Model
8.5/110
Catalog Number
510.701.111
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
b904d9d5-30af-4aac-a78d-d0acb37b545f

Device Description

Procedure Pack Ø 8.5mm,110µm flap thickness

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
HQF Laser, Ophthalmic

GMDN Terms

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

Identifiers

Type ID
Package 07640167750689
Primary 07640167750146

Customer Contacts

Phone
8667084490

Premarket Submissions

Submission Number Supplement Number
K053511 000
K112154 000

Device Sizes

Type Value Unit Text
Height 110 Micrometer
Lumen/Inner Diameter 8.5 Millimeter