FDA UDI In Commercial Distribution 🇺🇸 United States

FEMTO LDVᵀᴹ Intershields

DI: 07640167750856 · Model: d450 · SIE AG, Surgical Instrument Engineering
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
FEMTO LDVᵀᴹ Intershields
Primary DI
07640167750856
Version / Model
d450
Catalog Number
510.710.305
Company Name
SIE AG, Surgical Instrument Engineering
Labeler DUNS
482163628
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
c46d75bd-ae2b-4359-88e9-ffe0e2d48e4b

Device Description

Intershield d450 for LCS

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
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
HQF Laser, Ophthalmic

GMDN Terms

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

Identifiers

Type ID
Primary 07640167750856
Unit of Use 07640167750313

Customer Contacts

Phone
8667084490

Premarket Submissions

Submission Number Supplement Number
K112154 000

Device Sizes

Type Value Unit Text
Depth 450 Micrometer