Identity
- Trade Name
- Adapt CeraRing FDA UDI
- Generic Name
- Peristomal/periwound dressing FDA UDI
- Device Name
- Ostomy Barrier Ring, Convex FDA UDI
- Model / Reference
- 89530 FDA UDI
- Description
- Ostomy Barrier Ring, Convex FDA UDI
Identifiers
- Catalog Number
- 89530 FDA UDI
- Primary DI / UDI-DI
- 00610075060771 FDA UDI
- FDA Product Code
- EXE FDA UDI
- GMDN Term
- Peristomal/periwound dressing FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5900 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
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
Dimensions & Sizes
- Size
- Width — 30 Millimeter FDA UDI
Category: Peristomal/periwound dressing
Adapt CeraRing by Hollister Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peristomal/periwound dressing.
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- Brava — Coloplast A/S · Class I
- Safe N Simple — SAFE N SIMPLE LLC · Class I
- Brava — Coloplast A/S · Class I
- Brava — Coloplast A/S · Class I
- Eakin — T.G. EAKIN LIMITED · Class I
- Bynex — Zhende Medical Co., Ltd. · Class I
- Halyard — O&M HALYARD, 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
- Hollister Incorporated
Sources (1)
- FDA UDI ac1db1e8-0494-4622-955b-490a1ea104be 36 fields · synced Jun 9, 2026