FDA UDI In Commercial Distribution 🇺🇸 United States

Peregrine Surgical

DI: 00190660196486 · Model: Dugel trocar placement device - Sold exclusively through Peregrine Surgical · AMBLER SURGICAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Peregrine Surgical
Primary DI
00190660196486
Version / Model
Dugel trocar placement device - Sold exclusively through Peregrine Surgical
Catalog Number
DEP-Dugel
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
acc990b4-e19c-4a92-ad5c-594648588ce3

Device Description

Dugel trocar placement device - Sold exclusively through Peregrine Surgical

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
HND Spatula, ophthalmic

GMDN Terms

Code Name
32754 Ocular hook/spatula/manipulator, reusable

Identifiers

Type ID
Primary 00190660196486

Customer Contacts

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