FDA UDI
In Commercial Distribution
🇺🇸 United States
N/A
DI: 00382903024353
·
Model: 302435
·
BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- N/A
- Primary DI
- 00382903024353
- Version / Model
- 302435
- Catalog Number
- 302435
- Company Name
- BECTON, DICKINSON AND COMPANY
- Labeler DUNS
- 001292192
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-16
- Public Version
- 5
- Public Version Date
- 2025-08-06
- Public Version Status
- Update
- Public Device Record Key
- 0b996b03-3ef8-431f-88f7-31d8303bb6fc
Device Description
TIP CAP ENTERAL SYRINGES STERILE
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
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- Yes
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) | Gastroenterology, Urology | 876.5980 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 65151 | Non-ISO80369-standardized fluid path protective cover | A small, noninvasive, closed-ended attachment not designed according to ISO 80369 (non-ISO80369-standardized) intended to cover and close off (cap/plug) a luminal device associated with management of fluids (e.g., urological catheter, administration set, bag access spike). It is designed with a connection that is typically barbed, bayonet, collet, conical, threaded and/or non-Luer-slip; it is not intended to be used with respiratory or surgical equipment. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00382903024353 | GS1 | ||||
| Package | 50382903024358 | GS1 | Case | 10 | In Commercial Distribution | |
| Package | 30382903024354 | GS1 | Pack or Inner Pack | 100 | In Commercial Distribution |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K112434 | 000 |