FDA UDI In Commercial Distribution 🇺🇸 United States

Plastic Thumb Forceps

DI: 00616784491738 · Model: 4917 · DYNAREX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3000

Basic Information

Brand Name
Plastic Thumb Forceps
Primary DI
00616784491738
Version / Model
4917
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
3000
Record Status
Published
Publish Date
2021-06-21
Public Version
1
Public Version Date
2021-06-29
Public Version Status
New
Public Device Record Key
bb02d4cc-78e9-495e-aebb-e12ef33df8c0

Device Description

Plastic Thumb Forceps, 4.25", 12 Bags of 250

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HTD Forceps

GMDN Terms

Code Name
62479 Surgical soft-tissue manipulation forceps, tweezers-like, single-use

Identifiers

Type ID
Unit of Use 00616784491721
Primary 00616784491738