FDA UDI In Commercial Distribution 🇺🇸 United States

aScope™ 4 RhinoLaryngo Slim

DI: 05707480157983 · Model: 510177000 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
aScope™ 4 RhinoLaryngo Slim
Primary DI
05707480157983
Version / Model
510177000
Catalog Number
510177000
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-21
Public Version
1
Public Version Date
2022-09-29
Public Version Status
New
Public Device Record Key
86a6ec12-1b6a-4aa3-8d39-87f8c9fe655d

Device Description

aScope 4 RhinoLaryngo Slim Bosma

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EOB Nasopharyngoscope (flexible or rigid)

GMDN Terms

Code Name
63330 Flexible video otorhinolaryngoscope, single-use

Identifiers

Type ID
Package 05707480158003
Package 05707480157990
Primary 05707480157983

Customer Contacts

Phone
+14107686464