Identity
- Trade Name
- 3M™ Tegaderm™ FDA UDI
- Generic Name
- Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
- Device Name
- 1882 TEGADERM I.V. ADV 2-3 4X3-3 8 FDA UDI
- Model / Reference
- 1882 FDA UDI
- Description
- 1882 TEGADERM I.V. ADV 2-3 4X3-3 8 FDA UDI
Identifiers
- Catalog Number
- 1882 FDA UDI
- Primary DI / UDI-DI
- 04054596595910 FDA UDI
- FDA Product Code
- KMK FDA UDI
- GMDN Term
- Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5210 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
No
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
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: Synthetic polymer semi-permeable film dressing, adhesive
3M™ Tegaderm™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Synthetic polymer semi-permeable film dressing, adhesive.
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- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Mepore® Film — Mölnlycke Health Care AB · Class I
- Bedal — Bedal · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI f9ace23a-019f-4f5d-aad5-6dc3e04ad94b 35 fields · synced Jun 8, 2026