FDA UDI In Commercial Distribution 🇺🇸 United States

eyeMAX(TM) Single-Use Biopsy Forceps

DI: 46932503549347 · Model: BF16004 · Micro-Tech (Nanjing) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
eyeMAX(TM) Single-Use Biopsy Forceps
Primary DI
46932503549347
Version / Model
BF16004
Company Name
Micro-Tech (Nanjing) Co., Ltd.
Labeler DUNS
530269083
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-28
Public Version
4
Public Version Date
2025-12-02
Public Version Status
Update
Public Device Record Key
c1bac359-7937-4f27-9ddc-ca91f6203cdf

Device Description

"Two Wire,Alligator forceps. PE coating.1.6*2300mm "

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
FCL Forceps, Biopsy, Non-Electric

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Primary 46932503549347
Package 56932503549344
Package 66932503549341

Customer Contacts

Phone
877-552-4027

Device Sizes

Type Value Unit Text
Length 2300 Millimeter
Outer Diameter 1.6 Millimeter