Identity
- Trade Name
- microMend FDA UDI
- Generic Name
- First aid kit, medicated FDA UDI
- Device Name
- Emergency Laceration Kit: 2 – microMend Closures 1/2 IN x 1 IN (12 mm x 28 mm); 1 – Antiseptic Wipe 5 IN x 7 IN (127 mm x 178 mm); 2 – Gauze Packages 2 IN x 2 IN (51 mm x 51 mm) FDA UDI
- Model / Reference
- M1S2K001 FDA UDI
- Description
- Emergency Laceration Kit: 2 – microMend Closures 1/2 IN x 1 IN (12 mm x 28 mm); 1 – Antiseptic Wipe 5 IN x 7 IN (127 mm x 178 mm); 2 – Gauze Packages 2 IN x 2 IN (51 mm x 51 mm) FDA UDI
Identifiers
- Catalog Number
- M1S2K001 FDA UDI
- Primary DI / UDI-DI
- 00850018777018 FDA UDI
- FDA Product Code
- LRR FDA UDI
- GMDN Term
- First aid kit, medicated FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
microMend by Kitotech Medical Inc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
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Manufacturer
- Manufacturer
- Kitotech Medical Inc
Sources (1)
- FDA UDI d628d694-b519-4d52-ab96-0ded5065e7a2 37 fields · synced May 30, 2026