FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660129941 · Model: Lewis rasp · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660129941
Version / Model
Lewis rasp
Catalog Number
69-400
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
dd2d1544-17cc-41e5-a8d1-eb6daa9eb0a8

Device Description

Lewis rasp, 7 1/2'', straight, backward cutting, 8.0mm wide, coarse teeth

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
KBA RASP, NASAL

GMDN Terms

Code Name
35296 Nasal file/rasp

Identifiers

Type ID
Primary 00190660129941

Customer Contacts

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