Identity
- Trade Name
- Medical Maggots FDA UDI
- Generic Name
- Wound debridement maggot FDA UDI
- Device Name
- Maggot-impregnated gauze. Two 2" x 2" gauze pads impregnated with 250 - 500 disinfected larvae. FDA UDI
- Model / Reference
- 250 FDA UDI
- Description
- Maggot-impregnated gauze. Two 2" x 2" gauze pads impregnated with 250 - 500 disinfected larvae. FDA UDI
Identifiers
- Catalog Number
- MM250 FDA UDI
- Primary DI / UDI-DI
- B698MM2500 FDA UDI
- 510(k) Number
- K033391 FDA UDI
- FDA Product Code
- NQK FDA UDI
- GMDN Term
- Wound debridement maggot FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wound debridement maggot
Medical Maggots by Monarch Labs, Llc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wound debridement maggot.
Cleared under the same submission
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 U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Monarch Labs, Llc.
Sources (1)
- FDA UDI bc2e381f-ac6a-4dbc-97e5-5978c33e1fb6 37 fields · synced May 30, 2026