FDA UDI
In Commercial Distribution
🇺🇸 United States
HWJECT AUTO-DISABLE SYRINGE
DI: 06958697621807
·
Model: 1 mL 22G x 38mm TWLB
·
ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER CO LTD
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
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Basic Information
- Brand Name
- HWJECT AUTO-DISABLE SYRINGE
- Primary DI
- 06958697621807
- Version / Model
- 1 mL 22G x 38mm TWLB
- Company Name
- ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER CO LTD
- Labeler DUNS
- 543007373
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2026-03-26
- Public Version
- 1
- Public Version Date
- 2026-04-03
- Public Version Status
- New
- Public Device Record Key
- e4c643cf-ecc8-404d-b103-51cf592628ee
Device Description
HWJECT AUTO-DISABLE SYRINGE 1 mL 22G x 38mm TWLB
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
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| FMF | Syringe, Piston | General Hospital | 880.5860 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 35904 | Metered-delivery hypodermic syringe | A sterile device consisting of a graduated barrel (cylinder) with plunger intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. The application of the content of this device may be in conjunction with an injector device (transcutaneous delivery) or through the traditional use of a needle (subcutaneous delivery). It may allow for retraction of an attached needle (safety syringe); the needle is not included. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 16958697621804 | GS1 | 100 | In Commercial Distribution | ||
| Primary | 06958697621807 | GS1 | ||||
| Package | 26958697621801 | GS1 | 2400 | In Commercial Distribution |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K234024 | 000 |