FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660093235 · Model: House tympanoplasty knife · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660093235
Version / Model
House tympanoplasty knife
Catalog Number
39-510
Company Name
AMBLER SURGICAL CORP.
Labeler DUNS
015272206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-07
Public Version
1
Public Version Date
2021-01-15
Public Version Status
New
Public Device Record Key
bbda4a13-4b1e-42d1-990f-12d43d6f241e

Device Description

House tympanoplasty knife, 6 1/2'', straight shaft, curved, 7.0mm long blade, 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
KTG KNIFE, ENT

GMDN Terms

Code Name
37840 Cartilage knife

Identifiers

Type ID
Primary 00190660093235

Customer Contacts

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