FDA UDI
In Commercial Distribution
🇺🇸 United States
FORWARD AAJT-S Deployment Kit
DI: 00850056748001
·
Model: 1101-22000CB
·
Integrated Medcraft LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- FORWARD AAJT-S Deployment Kit
- Primary DI
- 00850056748001
- Version / Model
- 1101-22000CB
- Company Name
- Integrated Medcraft LLC
- Labeler DUNS
- 107523667
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2024-02-12
- Public Version
- 1
- Public Version Date
- 2024-02-20
- Public Version Status
- New
- Public Device Record Key
- fc075330-9663-41d7-96b0-be09f6b4669e
Device Description
FORWARD AAJT-S Deployment Kit includes AAJT-S Junctional Tourniquet and Carry Pouch.
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
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DXC | Clamp, Vascular | Cardiovascular | 870.4450 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 63268 | Emergency junctional haemorrhage compression set | A collection of non-sterile, noninvasive devices intended to be used in an emergency situation (e.g., battlefield) to provide compression for haemostasis to a traumatic wound occurring proximal to where a limb meets the torso/pelvis. Often referred to as a junctional tourniquet, it consists of a belt(s)/binder(s), an inflatable bulb(s), and a hand pump. The inflatable bulb is intended to be secured at the point of the wound with the belt, then inflated to provide compression and prevent bleeding. The belt component may be additionally intended to be used as a binder. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00850056748001 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K221661 | 000 |