FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660110307 · Model: Maxillary ostium seeker · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660110307
Version / Model
Maxillary ostium seeker
Catalog Number
44-950
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
1794eba9-0719-41a9-85ac-236cd97bf7cf

Device Description

Maxillary ostium seeker, 7 7/16'', double-ended, curved, 2.0mm and 2.6mm ball tips, hexagonal handle

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KAK PROBE, ENT

GMDN Terms

Code Name
35252 Fistula probe

Identifiers

Type ID
Primary 00190660110307

Customer Contacts

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