FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660039196 · Model: Ambler ear forceps · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660039196
Version / Model
Ambler ear forceps
Catalog Number
28-120RG
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
cdeea2e8-5b6e-4f5c-b29e-1d73f58c8b1b

Device Description

Ambler ear forceps, 5 1/4'', working length 70.0mm, very delicate, straight, 0.4mm oval cup jaws, ring handle, ebonized finish for reduced glare

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
KAE FORCEPS, ENT

GMDN Terms

Code Name
35802 Otologic clamp

Identifiers

Type ID
Primary 00190660039196

Customer Contacts

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