FDA UDI In Commercial Distribution 🇺🇸 United States

Amnihook Amniotic Membrane Perforator

DI: 00840113231485 · Model: 9601 · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Amnihook Amniotic Membrane Perforator
Primary DI
00840113231485
Version / Model
9601
Company Name
ASPEN SURGICAL PRODUCTS, INC.
Labeler DUNS
027680821
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-27
Public Version
1
Public Version Date
2023-03-07
Public Version Status
New
Public Device Record Key
14590b08-189f-4824-bf8d-f63276f1202a

Device Description

Stork AmniHook, Amniotic Membrane Perforator, Yellow, Sterile, 1/pouch, 100pouches/box

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HGE Amniotome

GMDN Terms

Code Name
46520 Amniotic membrane perforator, single-use

Identifiers

Type ID
Primary 00840113231485