Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- Tubular support bandage, non-latex, single-use FDA UDI
- Device Name
- BNDG,TUBLR,MEDIGRIP SZ C 2-5/8W,LF FDA UDI
- Model / Reference
- MSC9502LF FDA UDI
- Description
- BNDG,TUBLR,MEDIGRIP SZ C 2-5/8W,LF FDA UDI
Identifiers
- Catalog Number
- MSC9502LF FDA UDI
- Primary DI / UDI-DI
- 10888277718616 FDA UDI
- FDA Product Code
- MHW FDA UDI
- GMDN Term
- Tubular support bandage, non-latex, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5075 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Tubular support bandage, non-latex, single-use
Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Tubular support bandage, non-latex, single-use.
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- Juzo Bandaging Supplies — JULIUS ZORN, INC. · Class I
- NATIONAL HOSPITAL PACKAGING — Surgi-Pak, Inc. · Class I
- NATIONAL HOSPITAL PACKAGING — Surgi-Pak, Inc. · Class I
- NATIONAL HOSPITAL PACKAGING — Surgi-Pak, Inc. · Class I
- Juzo Bandaging Supplies — JULIUS ZORN, INC. · 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
- Medline Industries, Inc.
Sources (1)
- FDA UDI ea7447d4-23ed-4fa3-b112-bdf192909f50 35 fields · synced May 30, 2026