FDA UDI In Commercial Distribution 🇺🇸 United States

Backflush Instrument with 20 gauge / 0.9 mm blunt needle.

DI: 08717872026152 · Model: 2281.AD · D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Backflush Instrument with 20 gauge / 0.9 mm blunt needle.
Primary DI
08717872026152
Version / Model
2281.AD
Catalog Number
2281.AD
Company Name
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Labeler DUNS
407522184
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-02-11
Public Version
2
Public Version Date
2021-02-24
Public Version Status
Update
Public Device Record Key
b48f3339-93a0-4553-9455-fa8218ca4c8a

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
Yes
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
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
47130 Vitrectomy fluid/gas handling handpiece/cannula

Identifiers

Type ID
Unit of Use 18717872026159
Primary 08717872026152