FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660192228 · Model: Troutman corneal punch system replacement Teflon base block · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660192228
Version / Model
Troutman corneal punch system replacement Teflon base block
Catalog Number
33-0001
Company Name
AMBLER SURGICAL CORP.
Labeler DUNS
015272206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-04
Public Version
1
Public Version Date
2021-01-12
Public Version Status
New
Public Device Record Key
a1c0130d-5029-45ad-a5df-5ba6aa480ecd

Device Description

Troutman corneal punch system replacement Teflon base block, packaged individually, sterile, disposable, box of 1, for use with 33-0010

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRH Trephine, manual, ophthalmic

GMDN Terms

Code Name
14148 Corneal trephine, reusable

Identifiers

Type ID
Primary 00190660192228

Customer Contacts

Phone
+1(888)407-0006 ext. 0