Identity
- Trade Name
- Arjo Wiggins Medical, Inc. FDA UDI
- Generic Name
- Sterilization packaging, single-use FDA UDI
- Device Name
- 47 ARJORAD 24X24 FDA UDI
- Model / Reference
- 101047AR2424 FDA UDI
- Description
- 47 ARJORAD 24X24 FDA UDI
Identifiers
- Catalog Number
- 101047AR2424 FDA UDI
- Primary DI / UDI-DI
- 00815588021367 FDA UDI
- 510(k) Number
- K062100 FDA UDI
- FDA Product Code
- FRG FDA UDI
- GMDN Term
- Sterilization packaging, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Arjo Wiggins Medical, Inc. by Sterimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K062100 also covers:
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- CSR Wraps — Dynarex Corp.
- Arjo Wiggins Medical, Inc. — Sterimed, Inc.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Sterimed, Inc.
Sources (1)
- FDA UDI 6943be11-531b-454d-9d65-311ae5e9716b 38 fields · synced Jun 1, 2026