FDA UDI In Commercial Distribution 🇺🇸 United States

Ambler Surgical

DI: 00190660173531 · Model: Outer sheath · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ambler Surgical
Primary DI
00190660173531
Version / Model
Outer sheath
Catalog Number
96-200
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
b5a4041a-808f-4313-86a9-8ac9a3c062c6

Device Description

Outer sheath, insulated, 5.0mm diameter, 210.0mm working length

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
FBM Cannula and trocar, suprapubic, non-disposable

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 00190660173531

Customer Contacts

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