Identity
- Trade Name
- DormDoc FDA UDI
- Generic Name
- First aid kit, medicated FDA UDI
- Model / Reference
- DD-175-Black-22 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860000737166 FDA UDI
- FDA Product Code
- LRR FDA UDI
- GMDN Term
- First aid kit, medicated FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, medicated
DormDoc by Mydormdoc, LLC — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as First aid kit, medicated.
- OP - First aid series — Yiwu Ori-Power Medtech Co., Ltd. · N
- American Red Cross — ACME UNITED CORP. · N
- OP - First aid series — Yiwu Ori-Power Medtech Co., Ltd. · N
- HSB - National Standard Body Fluid — Certified Safety Manufacturing, Inc. · N
- First Aid Only — Acme United Corporation · N
- First Aid Only — ACME UNITED CORP. · N
- NAR — NORTH AMERICAN RESCUE, LLC.
- OP - First aid series — Yiwu Ori-Power Medtech Co., Ltd. · N
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class N | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mydormdoc, LLC
Sources (1)
- FDA UDI 78798ff0-7216-4d7f-b844-e1ffe5f79faf 33 fields · synced May 30, 2026