Identity
- Trade Name
- LMP Manuka IG Max Rope FDA UDI
- Generic Name
- Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
- Device Name
- Honey-impregnated gauze wound dressing FDA UDI
- Model / Reference
- WC37 FDA UDI
- Description
- Honey-impregnated gauze wound dressing FDA UDI
Identifiers
- Catalog Number
- WC37 FDA UDI
- Primary DI / UDI-DI
- 00851028001377 FDA UDI
- 510(k) Number
- K120976 FDA UDI
- FDA Product Code
- FRO FDA UDI
- GMDN Term
- Wound-nonadherent dressing, absorbent, non-antimicrobial 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 1 Inch FDA UDILength — 12 Inch FDA UDI
Category: Wound-nonadherent dressing, absorbent, non-antimicrobial
LMP Manuka IG Max Rope by Links Medical Products, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.
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Cleared under the same submission
K120976 also covers:
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 |
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Manufacturer
- Manufacturer
- Links Medical Products, Inc.
Sources (1)
- FDA UDI 0338670b-187e-41d7-8a01-653e53c47f10 38 fields · synced Sep 18, 2026